Rhinopithecus roxellana (golden snub-nosed monkey): 104656476 Help Entry 104656476         CDS       T03989                                  Gene name WNT8B Definition (RefSeq) protein Wnt-8b   KO K00714   wingless-type MMTV integration site family, member 8 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104656476 (WNT8B)    04390 Hippo signaling pathway     104656476 (WNT8B)    04150 mTOR signaling pathway     104656476 (WNT8B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104656476 (WNT8B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104656476 (WNT8B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104656476 (WNT8B)    05205 Proteoglycans in cancer     104656476 (WNT8B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104656476 (WNT8B)    05226 Gastric cancer     104656476 (WNT8B)    05217 Basal cell carcinoma     104656476 (WNT8B)    05224 Breast cancer     104656476 (WNT8B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104656476 (WNT8B)    05022 Pathways of neurodegeneration - multiple diseases     104656476 (WNT8B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104656476 (WNT8B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104656476 (WNT8B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104656476 (WNT8B) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104656476 (WNT8B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104656476 NCBI-ProteinID:  XP_010354397 UniProt:  A0A2K6PYK0 LinkDB All DBs Position 11 AA seq 351 aa AA seqDB search MFLSKPSVYISLFTCVLQLSHSWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAW DRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNG QLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTC KCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRS ISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEE RRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKP NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atgtttctttcaaagccttctgtgtacatctctcttttcacctgtgtcctccaactcagc cacagctggtcagtgaacaatttcctgatgactggtccaaaggcttacctgatttactcc agcagtgtggcagctggtgcccagagtggtattgaagaatgcaagtatcagtttgcctgg gaccgctggaactgccctgagagagctctgcagctgtccagccatggtgggcttcgcagt gctaatcgggagacagcatttgtgcatgccatcagttctgctggagtcatgtacaccctg actagaaactgcagccttggagattttgataactgtggctgtgatgactcccgcaatggg caactggggggccaaggctggctgtggggaggctgcagcgacaatgtgggcttcggagag gcgatttccaagcagtttgtcgatgccctggaaacaggacaggatgcacgggcagccatg aacctgcacaacaacgaggctggccgcaaggcggtgaagggcaccatgaaacgtacgtgc aagtgccacggcgtgtctggcagctgcaccacgcagacctgttggctgcagctgcccgag ttccgcgaggtgggcgcgcacctgaaggagaagtaccacgcagcactcaaggtagacctg ctgcagggtgctggcaacagcgctgccggccgcggcgccatcgccgacacctttcgctcc atctccacccgggagctggtgcacctggaggactccccggactactgcctggagaacaaa acgctaggactgctgggcaccgaaggccgagagtgcctgaggcgcgggcgggccctgggt cgctgggaacgccgcagctgccgccggctctgcggggactgcgggctggcggtggaggag cgccgggccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgcagtccgc tgcgagcagtgccgccggcgggtcaccaagtacttctgcagccgcgcagagcggccgcgg gggggcgctgcgcacaaacccgggagaaaaccctaa

Rhinopithecus roxellana (golden snub-nosed monkey): 104658925 Help Entry 104658925         CDS       T03989                                  Gene name WNT2B Definition (RefSeq) protein Wnt-2b   KO K00182   wingless-type MMTV integration site family, member 2 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104658925 (WNT2B)    04390 Hippo signaling pathway     104658925 (WNT2B)    04150 mTOR signaling pathway     104658925 (WNT2B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104658925 (WNT2B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104658925 (WNT2B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104658925 (WNT2B)    05205 Proteoglycans in cancer     104658925 (WNT2B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104658925 (WNT2B)    05226 Gastric cancer     104658925 (WNT2B)    05217 Basal cell carcinoma     104658925 (WNT2B)    05224 Breast cancer     104658925 (WNT2B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104658925 (WNT2B)    05022 Pathways of neurodegeneration - multiple diseases     104658925 (WNT2B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104658925 (WNT2B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104658925 (WNT2B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104658925 (WNT2B) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104658925 (WNT2B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104658925 NCBI-ProteinID:  XP_010357366 UniProt:  A0A2K6PN62 LinkDB All DBs Position 8 AA seq 391 aa AA seqDB search MLRPGGAEEAAQLPLRRARAPVPVPSPAVPDGSRASARLGLACLLLLLLLTLPARVDTSW WYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNCTT LDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHDQR GDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCH GVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVMATQDGANFTAARQGYRRATRTDLV YFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFH WCCAVRCKECRNTVDVHTCKAPKKAEWLDQT NT seq 1176 nt NT seq  +upstreamnt  +downstreamnt atgctgagaccgggtggtgcggaggaagctgcgcagctcccgcttcggcgcgcccgcgcc ccggtccctgtgccctcgcctgcggtccccgacggctcccgggcttcggcccgcctaggt cttgcctgccttctgctcctgctgctgctgacgctgccggcccgcgtagacacgtcctgg tggtacattggggcactgggggcacgagtgatctgtgacaatatccctggtttggtgagc cggcagcggcagctgtgccagcgttacccagacatcatgcgttcagtgggcgagggtgcc cgagaatggatccgagagtgtcagcaccaattccgccaccaccgctggaactgtaccacc ctggaccgggaccacactgtctttggccgtgtcatgctcagaagtagccgagaagcagct tttgtatatgccatctcatcagcaggggtagtccatgctattactcgtgcctgtagccag ggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgaccagcgt ggggactttgactggggtggctgcagtgacaacatccattatggtgtccgttttgccaag gccttcgtggatgccaaggagaagaggcttaaggatgcccgggccctcatgaacttacat aataaccgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgtaagtgccat ggcgtgagtggttcctgtactctgcgcacctgctggcgtgcgctctcagatttccgccgc acaggtgattacctgcggcggcgctatgatggggctgtgcaggtgatggccacgcaggat ggtgccaatttcaccgcagcccgccaaggctatcgccgtgccacccgaactgatcttgtc tactttgacaactccccagattactgtgtcttggacaaggctgcaggttccctaggcact gcaggccgtgtctgcagcaagacatcaaaaggaacagacggttgtgaaatcatgtgctgt ggtcgagggtatgacacaactcgagtcacccgtgttacccagtgtgagtgcaaattccac tggtgctgtgctgtacggtgcaaggaatgcagaaatactgtggatgtccatacttgcaag gcccccaagaaggcagagtggctggaccagacctga

Rhinopithecus roxellana (golden snub-nosed monkey): 104660036 Help Entry 104660036         CDS       T03989                                  Gene name WNT6 Definition (RefSeq) protein Wnt-6   KO K00445   wingless-type MMTV integration site family, member 6 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104660036 (WNT6)    04390 Hippo signaling pathway     104660036 (WNT6)    04150 mTOR signaling pathway     104660036 (WNT6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104660036 (WNT6)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104660036 (WNT6)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104660036 (WNT6)    05205 Proteoglycans in cancer     104660036 (WNT6)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104660036 (WNT6)    05226 Gastric cancer     104660036 (WNT6)    05217 Basal cell carcinoma     104660036 (WNT6)    05224 Breast cancer     104660036 (WNT6)   09164 Neurodegenerative disease    05010 Alzheimer disease     104660036 (WNT6)    05022 Pathways of neurodegeneration - multiple diseases     104660036 (WNT6)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104660036 (WNT6)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104660036 (WNT6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104660036 (WNT6) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104660036 (WNT6) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104660036 NCBI-ProteinID:  XP_030772493 LinkDB All DBs Position 14 AA seq 365 aa AA seqDB search MLPPAPSRLGLLLLLLLCPAHVGGLWWAVGSPLVMDPISICRKARRLAGRQAELCQAEPE VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV TQACSMGELLQCGCQAPRGRSPPRPSGLPGTPGPPGPVGSPEGSSAWEWGGCGDDVDFGD EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE LNLCL NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atgctgccgcccgcgccctcccgcctcgggctgctgctgctgctgctcctgtgcccagcg cacgtcggcggactgtggtgggctgtgggcagccccttggttatggatcctatcagcatc tgcaggaaggcacggcggctggccgggaggcaggctgagttgtgccaggctgagccggaa gtagtggcagagctagcccgaggcgcccggctcggggtgcgagagtgccagttccagttc cgcttccgccgctggaactgctccagccacagcaaggcctttggacgcatcctgcagcag gacattcgagagacggccttcgtgttcgccatcactgcggcgggcgccagccacgccgtc acgcaggcctgttccatgggcgagctgctgcagtgcggctgccaggcgccccgcgggcgg tcccctccccggccctctggcctgcccggcacccccggaccccctggccccgtgggctcc ccggaaggcagctctgcctgggagtggggaggctgcggcgacgacgtggacttcggggac gagaagtcgaggctctttatggacgcgcggcacaagcggggacgcggagacatccgcgcg ttggtgcaactgcacaacaacgaggcgggccggctggccgtgcggagccacacgcgcacc gagtgcaaatgccacgggctgtcgggctcgtgcgcgctgcgaacctgctggcagaagctg cctccatttcgcgaggtgggcgcgcggctgctggagcgcttccacggcgcctcacgcgtc atgggcactaacgacggcaaggccctactgccagccgtccgcacgctcaagccgccgggc cgagcggacctcctctacgccgctgattcgcccgacttctgcgcccccaaccgacgcacc ggctcccccggcacgcgcggccgcgcctgcaacagcagcgccccggacctcagtggttgc gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaagagaactgc ctgtgccgtttccactggtgctgcgtagtgcagtgccaccgctgccgtgtgcgcaaggag ctcaacctctgcctctga

Rhinopithecus roxellana (golden snub-nosed monkey): 104660037 Help Entry 104660037         CDS       T03989                                  Gene name WNT10A Definition (RefSeq) protein Wnt-10a   KO K01357   wingless-type MMTV integration site family, member 10 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104660037 (WNT10A)    04390 Hippo signaling pathway     104660037 (WNT10A)    04150 mTOR signaling pathway     104660037 (WNT10A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104660037 (WNT10A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104660037 (WNT10A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104660037 (WNT10A)    05205 Proteoglycans in cancer     104660037 (WNT10A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104660037 (WNT10A)    05226 Gastric cancer     104660037 (WNT10A)    05217 Basal cell carcinoma     104660037 (WNT10A)    05224 Breast cancer     104660037 (WNT10A)   09164 Neurodegenerative disease    05010 Alzheimer disease     104660037 (WNT10A)    05022 Pathways of neurodegeneration - multiple diseases     104660037 (WNT10A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104660037 (WNT10A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104660037 (WNT10A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104660037 (WNT10A) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104660037 (WNT10A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Ebola_NP Motif Other DBs NCBI-GeneID:  104660037 NCBI-ProteinID:  XP_010358561 UniProt:  A0A2K6PDT6 LinkDB All DBs Position 14 AA seq 417 aa AA seqDB search MGSAHPRPWLRLRPQPQPRPALWVLLFFLLLLAAAMPRSAPNDILDLRLPPEPVLNANTV CLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKIPYES PIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLKACGCDASRRGDEEAFRRKLHRLQLD ALQRGKGLSHGVPEHPALPTASPGLQDSWEWGGCSPDMGFGERFSKDFLDSREPHRDIHA RMRLHNNRVGRQAVMENMRRKCKCHGTSGSCQLKTCWQVTPEFRTVGALLRSRFHRATLI RPHNRNGGQLEPGPAGAPSPAPGAPGPRRRASPADLVYFEKSPDFCEREPRLDSAGTVGR LCNKSSAGSDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK NT seq 1254 nt NT seq  +upstreamnt  +downstreamnt atgggcagcgcccaccctcgcccctggctgcggctccgaccccagccccagccgcggcca gcgctctgggtgctcctgttcttcctactgctgctggctgctgccatgcccaggtcagca cccaatgacattctggacctccgcctccccccggagcctgtgctcaatgccaacacagtg tgcctaacattgccaggcctgagccggcggcagatggaggtgtgtgtgcgtcaccctgat gtggctgcctcagccatacagggcatccagatcgctatccacgaatgccaacaccaattc agggaccagcgctggaactgctcaagcctggagactcgcaacaagatcccctatgaaagt cccatcttcagcagaggtttccgagagagcgcttttgcctacgccatcgcggcagctggt gttgtacacgccgtgtccaatgcgtgtgccctgggcaaactaaaggcctgtggctgcgat gcctcccggcgaggggacgaggaggccttccgtaggaagctgcaccgcctacaactggac gcactgcagcgtggtaagggcctgagccatggggtcccggaacacccagccctgcccaca gccagcccaggcctgcaggactcctgggagtggggcggctgcagccccgacatgggcttc ggggagcgcttctctaaggactttctggactcccgggagcctcacagagacatccacgca agaatgaggcttcacaacaaccgagttgggagacaggcagtgatggagaacatgcggcga aagtgcaagtgccacggcacgtcaggcagctgccagctcaagacgtgctggcaggtgacg cccgagttccgcaccgtgggggcgctgctgcgcagccgcttccaccgcgccacgctcatc cggccgcacaaccgcaacggcggccagctggagccgggcccagcgggggcaccctcgccg gctcccggagctcccgggccgcgccgccgggccagccccgccgacctggtctacttcgaa aagtcacccgacttctgcgagcgcgagccgcgcctggactcggcgggcaccgtgggccgc ctgtgcaacaagagcagcgcgggctcggatggctgcggcagcatgtgttgcggccgcggc cacaacatcctgcgccagacgcgcagcgagcgctgccactgccgcttccactggtgctgc ttcgtggtctgcgaagagtgccgcatcaccgagtgggtcagcgtctgcaagtga

Rhinopithecus roxellana (golden snub-nosed monkey): 104662531 Help Entry 104662531         CDS       T03989                                  Gene name WNT5B Definition (RefSeq) protein Wnt-5b   KO K00444   wingless-type MMTV integration site family, member 5 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04360   Axon guidance rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104662531 (WNT5B)    04390 Hippo signaling pathway     104662531 (WNT5B)    04150 mTOR signaling pathway     104662531 (WNT5B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104662531 (WNT5B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104662531 (WNT5B)   09158 Development and regeneration    04360 Axon guidance     104662531 (WNT5B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104662531 (WNT5B)    05205 Proteoglycans in cancer     104662531 (WNT5B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104662531 (WNT5B)    05226 Gastric cancer     104662531 (WNT5B)    05217 Basal cell carcinoma     104662531 (WNT5B)    05224 Breast cancer     104662531 (WNT5B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104662531 (WNT5B)    05022 Pathways of neurodegeneration - multiple diseases     104662531 (WNT5B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104662531 (WNT5B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104662531 (WNT5B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104662531 (WNT5B) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104662531 (WNT5B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104662531 NCBI-ProteinID:  XP_010361861 UniProt:  A0A2K6RWI3 LinkDB All DBs Position 10 AA seq 359 aa AA seqDB search MPSLLLLFTAALLSSWAQLLTDANSWWSLALNPVQRPEMFIIGAQPVCSQLPGLSPGQRK LCQLYQEHMAYIGEGAKTGIKECQHQFRQRRWNCSTVDNVSVFGRVMQIGSRETAFTYAV SAAGVVNAISRACREGELSTCGCSRTARPKDLPRDWLWGGCGDNVEYGYRFAKEFVDARE REKNFAKGSEEQGRVLMNLQNNEAGRRAVYKMADVACKCHGVSGSCSLKTCWLQLAEFRK VGDRLKEKYDSAAAMRVTRRGRLELVNSRFTQPTPEDLVYVDPSPDYCLRNESTGSLGTQ GRLCNKTSEGMDGCELMCCGRGYNQFKSVQVERCHCKFHWCCFVKCKKCTEIVDQYICK NT seq 1080 nt NT seq  +upstreamnt  +downstreamnt atgcccagcctgctgctgctgttcacggctgccctgctgtccagctgggctcagcttctg acagacgccaactcctggtggtcattagctctgaacccggtgcagagacccgagatgttt atcatcggtgcccagcccgtgtgcagtcagcttcctgggctctcccctggccagaggaag ctgtgccaactgtaccaggagcacatggcctacataggggagggagccaagacaggcatc aaggagtgccagcaccagttccggcagcggcggtggaactgcagcacggtggacaacgtg tctgtctttgggagagtcatgcagataggtagccgtgagaccgccttcacctatgcagtg agcgccgcaggcgtggtcaacgccatcagccgggcctgtcgggagggcgagctctccacc tgcggctgcagccggaccgcgcggcccaaggacctgccccgggactggctgtggggtggc tgtggggacaatgtggagtacggctaccgcttcgccaaggagtttgtggatgcccgggag cgagagaagaactttgccaaaggatcagaggaacagggccgggtgctcatgaatctgcag aacaacgaggcgggtcgcagggctgtgtataagatggcggacgtagcctgcaaatgccac ggcgtctcggggtcctgcagcctcaagacctgctggctgcagctggccgagttccgcaag gtgggggaccggctgaaggagaagtatgacagcgcggccgccatgcgcgtcacccgcagg ggccggctggagctggtcaacagccgcttcacccagcccaccccagaggacctggtctac gtggaccccagccctgactactgcctgcgcaacgagagcacgggctccctgggcacgcag ggtcgtctctgcaacaagacctcggagggcatggatggctgtgagctcatgtgctgcggg cgtggctacaaccagttcaagagcgtgcaggtggagcgctgccactgcaagttccactgg tgctgcttcgtcaagtgcaagaagtgcaccgagatcgtggaccagtacatctgtaaatag

Rhinopithecus roxellana (golden snub-nosed monkey): 104663222 Help Entry 104663222         CDS       T03989                                  Gene name WNT4 Definition (RefSeq) protein Wnt-4   KO K00408   wingless-type MMTV integration site family, member 4 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04360   Axon guidance rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04919   Thyroid hormone signaling pathway rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104663222 (WNT4)    04390 Hippo signaling pathway     104663222 (WNT4)    04150 mTOR signaling pathway     104663222 (WNT4)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104663222 (WNT4)  09150 Organismal Systems   09152 Endocrine system    04919 Thyroid hormone signaling pathway     104663222 (WNT4)    04916 Melanogenesis     104663222 (WNT4)   09158 Development and regeneration    04360 Axon guidance     104663222 (WNT4)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104663222 (WNT4)    05205 Proteoglycans in cancer     104663222 (WNT4)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104663222 (WNT4)    05226 Gastric cancer     104663222 (WNT4)    05217 Basal cell carcinoma     104663222 (WNT4)    05224 Breast cancer     104663222 (WNT4)   09164 Neurodegenerative disease    05010 Alzheimer disease     104663222 (WNT4)    05022 Pathways of neurodegeneration - multiple diseases     104663222 (WNT4)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104663222 (WNT4)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104663222 (WNT4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104663222 (WNT4) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104663222 (WNT4) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt MEF2_binding Motif Other DBs NCBI-GeneID:  104663222 NCBI-ProteinID:  XP_030769562 LinkDB All DBs Position 12 AA seq 351 aa AA seqDB search MSPRSCLRSLRLLVFAVFSAAASNWLYLAKLSSVGSISEEETCEKLKGLIQRQVQMCKRN LEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAISSAGV AFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRERSKGAS SSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALKEKFDG ATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGTRGRTCNKTS KAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atgagtccccgctcctgcctgcgttcgctgcgcctcctcgtcttcgccgtcttctcagcc gccgcgagcaactggctgtacctggccaagctgtcgtcagtgggaagcatctcagaggag gagacgtgcgagaaactcaagggcctgatccagaggcaggtgcagatgtgcaagaggaac ctggaagtcatggactcggtgcgtcgcggtgcccaactggccattgaggagtgccagtac cagttccggaaccgacgctggaactgctccacactcgactccctgcccgtcttcggcaag gtggtgacgcaagggactcgggaggcggccttcgtgtacgccatctcttcggcaggtgtg gcctttgcagtgacacgggcgtgcagcagtggggagctggagaagtgtggctgtgaccgg acggtgcatggggtcagcccacagggcttccagtggtcaggatgctctgacaacatcgcc tacggtgtggccttctcacagtcgtttgtggatgtgcgggagagaagcaagggggcctcg tccagcagagccctcatgaacctccacaacaatgaggccggcaggaaggccatcctgaca cacatgcgggtggaatgcaagtgccacggggtgtcaggctcctgtgaggtaaagacgtgc tggcgagccgtgccgcccttccgccaggtgggtcacgcactgaaggagaagtttgatggt gccactgaggtggagccacgccgcgtgggctcctccagggcactggtgccacgcaatgca cagttcaagccacacacagatgaggacctggtgtacttggagcccagccctgacttctgc gagcaggacatgcgcagcggcgtgctgggcacaaggggccgcacatgcaacaagacgtcc aaggccatcgacggctgtgagctgctgtgctgtggccgcggcttccacacggcgcaggtg gagctggctgaacgctgcagctgcaaattccactggtgctgcttcgtcaagtgccggcag tgccagcggctcgtggagttgcacacgtgccgatga

Rhinopithecus roxellana (golden snub-nosed monkey): 104665095 Help Entry 104665095         CDS       T03989                                  Gene name WNT11 Definition (RefSeq) protein Wnt-11 isoform X3   KO K01384   wingless-type MMTV integration site family, member 11 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104665095 (WNT11)    04390 Hippo signaling pathway     104665095 (WNT11)    04150 mTOR signaling pathway     104665095 (WNT11)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104665095 (WNT11)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104665095 (WNT11)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104665095 (WNT11)    05205 Proteoglycans in cancer     104665095 (WNT11)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104665095 (WNT11)    05226 Gastric cancer     104665095 (WNT11)    05217 Basal cell carcinoma     104665095 (WNT11)    05224 Breast cancer     104665095 (WNT11)   09164 Neurodegenerative disease    05010 Alzheimer disease     104665095 (WNT11)    05022 Pathways of neurodegeneration - multiple diseases     104665095 (WNT11)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104665095 (WNT11)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104665095 (WNT11)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104665095 (WNT11) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104665095 (WNT11) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104665095 NCBI-ProteinID:  XP_010365085 UniProt:  A0A2K6PAX4 LinkDB All DBs Position 15 AA seq 354 aa AA seqDB search MRARPQVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR SNLELMHTVVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK NT seq 1065 nt NT seq  +upstreamnt  +downstreamnt atgagggcgcggccgcaggtctgcgaggcgctgctcttcgccctggcgctccagaccggc gtgtgctatggcatcaagtggctggcactgtccaagacaccagcagccctggcactgaac cagacacaacactgcaagcagctggagggcctggtgtctgcacaggtgcagctgtgccgc agcaacctggagctcatgcacacggtggtgcacgctgcccgcgaggtcatgaaggcctgt cgccgggccttcgccgacatgcgctggaactgctcctccattgagctcgcccccaactat ttgcttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggccgcc gccatcagccacgccatcgcccgggcctgcacctccggcgacctgccgggctgctcctgc ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct ctgcgcgcctctctggaaatgaagtgtaagtgccatggggtgtctggctcctgctccatc cgcacctgctggaaggggctgcaggagctacgggatgtggctgctgacctcaagacccga tacctgtcggccaccaaggtagtgcaccgacccatgggcacccgcaagcacctggtgccc aaagacctggatatccggcctgtgaaggactcagaactcgtctacctgcagagctcacct gacttctgcatgaagaatgagaaggtgggctcccatggaacacaagacaggcagtgcaac aagacatccaatggaagtgacagctgcgatcttatgtgctgtgggcgtggctacaacccc tatacagaccgcgtggtcgagcggtgccactgtaagtaccactggtgctgctacgtcacc tgccgcaggtgtgagcgtaccgtggagcgctatgtctgcaagtga

Rhinopithecus roxellana (golden snub-nosed monkey): 104672033 Help Entry 104672033         CDS       T03989                                  Gene name WNT9A Definition (RefSeq) protein Wnt-9a isoform X2   KO K01064   wingless-type MMTV integration site family, member 9 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104672033 (WNT9A)    04390 Hippo signaling pathway     104672033 (WNT9A)    04150 mTOR signaling pathway     104672033 (WNT9A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104672033 (WNT9A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104672033 (WNT9A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104672033 (WNT9A)    05205 Proteoglycans in cancer     104672033 (WNT9A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104672033 (WNT9A)    05226 Gastric cancer     104672033 (WNT9A)    05217 Basal cell carcinoma     104672033 (WNT9A)    05224 Breast cancer     104672033 (WNT9A)   09164 Neurodegenerative disease    05010 Alzheimer disease     104672033 (WNT9A)    05022 Pathways of neurodegeneration - multiple diseases     104672033 (WNT9A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104672033 (WNT9A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104672033 (WNT9A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104672033 (WNT9A) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104672033 (WNT9A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104672033 NCBI-ProteinID:  XP_010374009 UniProt:  A0A2K6PBW8 LinkDB All DBs Position 8 AA seq 365 aa AA seqDB search MLDGSPLARWLAAAFGLTLLLAALRPSAAYFGLTGSEPLTVLPLTLEPEAAAQAHYKACD RLKLERKQRRMCRRDPGVAETLVEAVSMSALECQFQFRFERWNCTLEGRYRASLLKRGFK ETAFLYAISSAGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVK EFLGRRSSKDLRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVG KHLKHKYETALKVGSTTNEAAGEAGAISPPRGRASGAGGSDPLPRTPELVHLDDSPSFCL AGRFSPGTAGRRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEV YTCKG NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atgctggatgggtccccgctggcgcgctggctggccgcggccttcgggctgacgctgctg ctcgccgcgctgcgcccttctgccgcctacttcgggctgacgggcagcgagcccctgact gtcctcccgctgaccctggagcccgaggcggccgcccaggcacactacaaggcctgcgac cggctgaagctggagcggaagcagcggcgcatgtgccgccgggacccgggtgtggcagag acgctggtggaggccgtgagcatgagtgcgcttgagtgccagttccagttccgctttgag cgctggaactgcacgctggagggccgctaccgggccagcctactcaagcgaggcttcaag gagactgccttcctctatgccatctcctcggctggcctgacgcacgcactggccaaggca tgcagcgcaggccgcatggagcgctgtacctgcgatgaggcgcccgacctggagaaccgt gaggcctggcagtgggggggctgcggagacaacctcaagtacagcagcaagttcgtcaag gagttcctgggcagacggtcaagcaaggatctgcgagcccgtgtggacttccacaacaac ctcgtgggtgtgaaggtgatcaaggctggggtggagaccacctgcaagtgccacggcgtg tcaggctcatgcacggtgcggacctgctggcggcagctggcgcccttccatgaggtgggc aagcacctgaagcacaagtatgagacagcactcaaggtgggcagcaccaccaacgaagct gcaggcgaggcaggcgccatttccccaccacggggccgtgcctcgggggcgggcggcagt gacccgctaccccgcactccagagctggtgcacctggacgactcgcctagcttctgcctg gccggccgcttctccccgggcaccgctggccgtaggtgccaccgcgagaagaactgcgag agcatctgctgcggccgcggccataacacacagagccgggtggtgacaaggccctgccag tgccaggtgcgttggtgctgctatgtggagtgcaggcagtgcacacagcgtgaggaggtc tacacctgcaagggctga

Rhinopithecus roxellana (golden snub-nosed monkey): 104672034 Help Entry 104672034         CDS       T03989                                  Gene name WNT3A Definition (RefSeq) protein Wnt-3a   KO K00312   wingless-type MMTV integration site family, member 3 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05206   MicroRNAs in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104672034 (WNT3A)    04390 Hippo signaling pathway     104672034 (WNT3A)    04150 mTOR signaling pathway     104672034 (WNT3A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104672034 (WNT3A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104672034 (WNT3A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104672034 (WNT3A)    05206 MicroRNAs in cancer     104672034 (WNT3A)    05205 Proteoglycans in cancer     104672034 (WNT3A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104672034 (WNT3A)    05226 Gastric cancer     104672034 (WNT3A)    05217 Basal cell carcinoma     104672034 (WNT3A)    05224 Breast cancer     104672034 (WNT3A)   09164 Neurodegenerative disease    05010 Alzheimer disease     104672034 (WNT3A)    05022 Pathways of neurodegeneration - multiple diseases     104672034 (WNT3A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104672034 (WNT3A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104672034 (WNT3A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104672034 (WNT3A) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104672034 (WNT3A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104672034 NCBI-ProteinID:  XP_010374010 UniProt:  A0A2K6QGF3 LinkDB All DBs Position 8 AA seq 352 aa AA seqDB search MAPLGYFLLLCSLKQALGSYPIWWSLAVGPQYSSLGSQPILCASIPGLVPKQLRFCRNYV EIMPSVAEGIKIGIQECQHQFRGRRWNCTTVHDSLAIFGPVLDKATRESAFVHAIASAGV AFAVTRSCAEGTAAICGCSSRNQGSPGKGWKWGGCSEDIEFGGMVSREFADARENRPDAR SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRAIGDFLKDKYDSASE MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVS SHGIDGCDLLCCGRGHNARAERRREKCRCVFHWCCYVSCQECTRVYDVHTCK NT seq 1059 nt NT seq  +upstreamnt  +downstreamnt atggccccgctcggatacttcttactcctctgcagcctgaagcaggctctgggcagctac ccgatctggtggtcgctggctgtcgggccacagtattcctccctgggctcacagcccatc ctgtgtgccagcattccaggcctggtccccaagcagctccgcttctgcaggaactacgtg gagatcatgcccagcgtggccgagggcatcaagattggcatccaggagtgccagcaccag ttccgcggccgccggtggaactgcaccaccgtccatgacagcctggccatcttcgggcct gtgctggacaaagctacgagggagtcagcctttgtccacgccattgcctcagctggtgtg gcctttgcggtgacacgctcatgtgcagagggcacggccgccatctgtggctgcagcagt cgcaaccagggctcaccaggcaagggctggaagtggggtggctgtagcgaggacatcgag tttggtgggatggtgtctcgggagttcgccgacgcccgggagaaccggccagatgcccgc tcagccatgaaccgccacaacaatgaggctgggcgccaggccatcgccagccacatgcac ctcaagtgcaagtgccacgggctgtcgggcagctgcgaggtgaagacttgctggtggtcg caacccgacttccgcgccattggtgacttcctcaaggacaagtacgacagcgcctcggag atggtggtggagaagcaccgggagtcccgcggatgggtggagaccctgcggccgcgctac acctacttcaaggtgcccacggagcgtgacctggtctactacgaggcctcgcccaacttc tgcgagcccaaccccgagacgggttccttcggcacgcgcgaccggacctgcaacgtcagc tcacacggcatcgacggctgcgacctgctgtgctgcggccgcggccacaacgcgagagcg gagcggcgccgggagaagtgccgctgcgtgttccactggtgctgctacgtcagctgccag gagtgcacgcgcgtctacgacgtgcacacctgcaagtag

Rhinopithecus roxellana (golden snub-nosed monkey): 104676099 Help Entry 104676099         CDS       T03989                                  Gene name WNT7B Definition (RefSeq) protein Wnt-7b isoform X1   KO K00572   wingless-type MMTV integration site family, member 7 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104676099 (WNT7B)    04390 Hippo signaling pathway     104676099 (WNT7B)    04150 mTOR signaling pathway     104676099 (WNT7B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104676099 (WNT7B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104676099 (WNT7B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104676099 (WNT7B)    05205 Proteoglycans in cancer     104676099 (WNT7B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104676099 (WNT7B)    05226 Gastric cancer     104676099 (WNT7B)    05217 Basal cell carcinoma     104676099 (WNT7B)    05224 Breast cancer     104676099 (WNT7B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104676099 (WNT7B)    05022 Pathways of neurodegeneration - multiple diseases     104676099 (WNT7B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104676099 (WNT7B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104676099 (WNT7B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104676099 (WNT7B) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104676099 (WNT7B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104676099 NCBI-ProteinID:  XP_030771622 LinkDB All DBs Position 13 AA seq 353 aa AA seqDB search MLLLSPRSALVSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP DAIIVIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA RRLMNLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR TSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK NT seq 1062 nt NT seq  +upstreamnt  +downstreamnt atgctcctactgtcgccgcgcagcgcgctcgtctctgtctattgcccgcagatctttctc ctcctgtccagcggcagctacctagcactgtcatcagtggtggccctgggagccaacatc atctgcaacaagattcctggcctagccccgcggcagcgtgccatctgccagagccggccc gatgccatcattgtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccag ttccgctttggacgctggaactgctctgccctcggcgagaagactgtctttgggcaagag ctccgagtagggagccgtgaggctgccttcacgtatgccatcaccgcggctggcgtagcg cacgccgtcactgccgcctgcagccaaggcaacctgagcaactgcggctgtgaccgcgag aagcagggctactacaaccaggccgagggctggaagtggggtggctgctcagccgacgtg cgttacggcatcgacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcg cggcgcctcatgaacctgcacaacaatgaggccggcaggaaggttctggaggaccggatg cagctggagtgcaagtgtcacggtgtgtctggctcctgcaccaccaagacctgctggacc acgctgcccaagttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtg caggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacag ctgcgcagctatcagaagcccatggagacggacctagtgtacatcgagaagtcgcccaac tactgcgaggaggacgcggccacgggaagcgtgggcactcagggccgcctctgcaaccgc acgtcgcccggtgcggacggctgtgacaccatgtgctgcggccgaggctacaacacccac cagtacaccaaggtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgc aacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

Rhinopithecus roxellana (golden snub-nosed monkey): 104676516 Help Entry 104676516         CDS       T03989                                  Gene name WNT5A Definition (RefSeq) protein Wnt-5a   KO K00444   wingless-type MMTV integration site family, member 5 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04360   Axon guidance rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104676516 (WNT5A)    04390 Hippo signaling pathway     104676516 (WNT5A)    04150 mTOR signaling pathway     104676516 (WNT5A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104676516 (WNT5A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104676516 (WNT5A)   09158 Development and regeneration    04360 Axon guidance     104676516 (WNT5A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104676516 (WNT5A)    05205 Proteoglycans in cancer     104676516 (WNT5A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104676516 (WNT5A)    05226 Gastric cancer     104676516 (WNT5A)    05217 Basal cell carcinoma     104676516 (WNT5A)    05224 Breast cancer     104676516 (WNT5A)   09164 Neurodegenerative disease    05010 Alzheimer disease     104676516 (WNT5A)    05022 Pathways of neurodegeneration - multiple diseases     104676516 (WNT5A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104676516 (WNT5A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104676516 (WNT5A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104676516 (WNT5A) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104676516 (WNT5A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104676516 NCBI-ProteinID:  XP_010379638 UniProt:  A0A2K6PGH6 LinkDB All DBs Position 1 AA seq 380 aa AA seqDB search MKKSIGILSPGVALGMAGSAVSSKFFLMALAIFFSFAQVVIEANSWWSLGMNNPVQMSEV YIIGAQPLCSQLAGLSQGQKKLCHLYQDHMQYIGEGAKTGIKECQYQFRHRRWNCSTVDN TSVFGRVMQIGSRETAFTYAVSAAGVVNAMSRACREGELSTCGCSRAARPKDLPRDWLWG GCGDNIDYGYRFAKEFVDARERERIHAKGSYESARILMNLHNNEAGRRTVYNLADVACKC HGVSGSCSLKTCWLQLADFRKVGDALKEKYDSAAAMRLNSRGKLVQVNSRFNSPTTQDLV YIDPSPDYCVRNESTGSLGTQGRLCNKTSEGMDGCELMCCGRGYDQFKTVQTERCHCKFH WCCYVKCKKCTEIVDQFVCK NT seq 1143 nt NT seq  +upstreamnt  +downstreamnt atgaagaagtccattggaatattaagcccaggagttgctttggggatggctggaagtgca gtgtcttccaagttcttcctaatggctttggccatatttttctccttcgcccaggttgta atagaagccaattcttggtggtcgctaggtatgaataaccctgttcagatgtcagaagta tatatcataggagcacagcctctctgcagccaactggcaggactttctcaaggacagaag aaactgtgccacttgtatcaggaccacatgcagtacatcggagaaggcgcgaagacaggc atcaaagagtgccagtatcaattccgacatcgaaggtggaactgcagcactgtggataac acctctgtttttggcagggtgatgcagataggcagccgcgagacggccttcacatacgcg gtgagcgcagcgggggtggtgaacgccatgagccgggcgtgccgcgagggcgagctgtcc acctgcggctgcagccgcgccgcgcgccccaaggacctgccgcgggactggctctggggc ggctgcggcgacaacatcgactatggctaccgctttgccaaggagttcgtggacgcccgc gagcgggagcgcatccacgccaagggctcctacgagagcgctcgcatcctcatgaacctg cataacaacgaggcaggccgcaggacggtgtacaacctggctgatgtggcctgcaagtgc catggggtgtctggctcatgtagcctgaagacatgctggctgcagttggcggacttccgc aaggtgggtgatgccctgaaggagaagtacgacagtgcggcggccatgcggctcaacagc cggggcaagttggtgcaggtcaacagccgcttcaactcgcccaccacacaagacctggtc tacatcgaccccagccctgactactgcgtgcgcaacgagagcaccggctcgctgggcacg cagggccgcctgtgcaacaagacgtcggagggcatggatggctgcgagctcatgtgctgc ggccgcggctacgaccagttcaagaccgtgcagacggagcgctgccactgcaagttccac tggtgctgctacgtcaagtgcaagaagtgcacggagatcgtggaccagtttgtgtgcaag tag

Rhinopithecus roxellana (golden snub-nosed monkey): 104677318 Help Entry 104677318         CDS       T03989                                  Gene name WNT16 Definition (RefSeq) LOW QUALITY PROTEIN: protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05202   Transcriptional misregulation in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104677318 (WNT16)    04390 Hippo signaling pathway     104677318 (WNT16)    04150 mTOR signaling pathway     104677318 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104677318 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104677318 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104677318 (WNT16)    05202 Transcriptional misregulation in cancer     104677318 (WNT16)    05205 Proteoglycans in cancer     104677318 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104677318 (WNT16)    05226 Gastric cancer     104677318 (WNT16)    05217 Basal cell carcinoma     104677318 (WNT16)    05224 Breast cancer     104677318 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     104677318 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     104677318 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104677318 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104677318 (WNT16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104677318 (WNT16) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104677318 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104677318 NCBI-ProteinID:  XP_010380607 UniProt:  A0A2K6PIA1 LinkDB All DBs Position 6 AA seq 365 aa AA seqDB search MDRAALLGLARLCALWAALLVLFPYGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC KRKPYLLPSIGEGARLGIQECRSQFRHERWNCMITAAATTAPMGASPLFGYELSSGTKET AFIYAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMRFSR KFLDFPXRNTTGKENKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMS SFEKIGHLLKDKYENSIQISDKIKRKMRRREKDQRKIPIHKDDLLYVNKSPNYCVEDKKL GIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTD VHTCK NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atggacagggcggcgctcctgggactggcccgcctgtgcgcgctgtgggcagccctgctc gtgctgttcccctacggagcccaaggaaactggatgtggttgggcattgcctccttcggg gttccagagaagctgggctgcgccaatttaccgctgaacagccgccagaaggagctgtgc aagaggaagccgtacctgctgccgagcatcggagagggcgcccggctgggcattcaggag tgcaggagtcagttcagacacgagagatggaactgcatgatcaccgctgccgccaccact gccccgatgggcgccagccccctctttggctacgagctgagcagcggcaccaaagagaca gcatttatttatgctgttatggctgcaggcctggtgcattctgtgaccaggtcatgcagt gcaggcaacatgacagagtgttcctgtgacaccaccttgcagaacggcggctcagcaagt gaaggatggcactgggggggctgctccgatgatgtccagtatggcatgcggttcagcaga aagttcctagatttcccantcagaaacaccacgggcaaagaaaacaaagtactattagca atgaacctacataacaatgaagctggaaggcaggctgtcgccaagttgatgtcagtagac tgccgctgccacggagtttccggctcctgtgctgtgaaaacatgctggaaaaccatgtct tcttttgaaaagattggccatttgttgaaggataaatatgaaaacagtatccaaatatca gacaaaataaagaggaaaatgcgcaggagagaaaaagatcagaggaaaataccaatccac aaggatgatctgctctatgttaataagtctcccaactactgtgtagaagataagaaactg ggaatcccagggacacaaggcagagaatgcaaccgtacatcagagggtgcagatggctgc aacctcctctgctgtggccgaggttacaacacccacgtggtccggcacgtggagaggtgt gagtgtaagttcatctggtgctgctatgtccgttgcaggaggtgtgaaagcatgactgat gtccacacttgcaagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 104679020 Help Entry 104679020         CDS       T03989                                  Gene name WNT7A Definition (RefSeq) protein Wnt-7a   KO K00572   wingless-type MMTV integration site family, member 7 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104679020 (WNT7A)    04390 Hippo signaling pathway     104679020 (WNT7A)    04150 mTOR signaling pathway     104679020 (WNT7A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104679020 (WNT7A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104679020 (WNT7A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104679020 (WNT7A)    05205 Proteoglycans in cancer     104679020 (WNT7A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104679020 (WNT7A)    05226 Gastric cancer     104679020 (WNT7A)    05217 Basal cell carcinoma     104679020 (WNT7A)    05224 Breast cancer     104679020 (WNT7A)   09164 Neurodegenerative disease    05010 Alzheimer disease     104679020 (WNT7A)    05022 Pathways of neurodegeneration - multiple diseases     104679020 (WNT7A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104679020 (WNT7A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104679020 (WNT7A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104679020 (WNT7A) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104679020 (WNT7A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt COG6 Motif Other DBs NCBI-GeneID:  104679020 NCBI-ProteinID:  XP_010382776 UniProt:  A0A2K6RP84 LinkDB All DBs Position 1 AA seq 349 aa AA seqDB search MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac ctccggatcggtggcttctcctcagtggtagctctgggcgcaagcatcatctgtaacaag atcccaggcctagctcctagacagcgggcgatctgccagagccggcccgacgccatcatc gtcataggagaaggctcgcaaatgggcctggacgagtgtcagtttcagttccgcaatggc cgctggaactgctctgcactgggagagcgcactgtcttcgggaaggagctgaaagtgggg agccgggaggctgcgttcacctacgccatcattgctgccggcgtggcccatgccatcaca gctgcctgtacccagggcaacctaagcgactgtggctgcgacaaagagaagcaaggccag taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg aacttgcacaataacgaggcaggccgaaagatcctggaggagaacatgaagctggaatgt aagtgccacggcgtgtcaggctcgtgcaccaccaagacgtgctggaccacactgccacag tttcgggagctgggctacgtgctcaaggacaagtacaacgaggccgttcacgtggagcct gtgcgtgccagccgcaacaagaggcccaccttcctgaagatcaagaagccactgtcatac cgcaagcccatggacacagacctggtgtacatcgagaagtcgcccaactactgcgaggag gacccggtgaccggcagtgtgggcacccagggccgcgcctgcaacaagacggccccccag gccagtggctgtgacctcatgtgctgtgggcgtggctacaacacccaccagtacgcccgt gtgtggcagtgcaactgtaagttccactggtgctgctatgtcaagtgcaacacgtgcagc gagcgcacggagatgtacacgtgcaagtga

Rhinopithecus roxellana (golden snub-nosed monkey): 104679729 Help Entry 104679729         CDS       T03989                                  Gene name WNT1 Definition (RefSeq) proto-oncogene Wnt-1   KO K03209   wingless-type MMTV integration site family, member 1 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104679729 (WNT1)    04390 Hippo signaling pathway     104679729 (WNT1)    04150 mTOR signaling pathway     104679729 (WNT1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104679729 (WNT1)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104679729 (WNT1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104679729 (WNT1)    05205 Proteoglycans in cancer     104679729 (WNT1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104679729 (WNT1)    05226 Gastric cancer     104679729 (WNT1)    05217 Basal cell carcinoma     104679729 (WNT1)    05224 Breast cancer     104679729 (WNT1)   09164 Neurodegenerative disease    05010 Alzheimer disease     104679729 (WNT1)    05022 Pathways of neurodegeneration - multiple diseases     104679729 (WNT1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104679729 (WNT1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104679729 (WNT1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104679729 (WNT1) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104679729 (WNT1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104679729 NCBI-ProteinID:  XP_010383724 UniProt:  A0A2K6NBC9 LinkDB All DBs Position 10 AA seq 370 aa AA seqDB search MGLWALLPGWVSATLLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTAPGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRVLHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggctctgggcgctgttgcctggctgggtttctgctacgctgctactggcgctggcc gctctgcccgcagctctggctgccaacagcagtggccgatggtggggtattgtgaacgta gcctcctccacgaacctgctgacggactccaagagtctgcaactggtactcgagcccagt ctgcagctgttgagccgcaaacagcggcgtctgatacgccaaaatccggggatcctgcac agcgtgagtggggggctacagagtgccgtgcgcgagtgcaagtggcagttccggaatcgc cgctggaactgtcccactgctccagggccccacctcttcggcaagatcgtcaaccgaggc tgtcgagaaacggcgtttatcttcgctatcacctccgccggggttacccattcggtggcg cgctcctgctcagagggttccatcgaatcctgcacgtgtgactaccggcggcgcggcccc gggggccccgactggcactgggggggctgcagcgacaacattgacttcggccgcctcttc ggccgggagttcgtggactccggggagaaggggcgggacctgcgcttcctcatgaacctt cacaacaacgaggctggccgtacgactgtattctccgagatgcgccaggagtgcaagtgc cacgggatgtccggttcctgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc gccgtgggcgatgtgctgcgcgaccgcttcgacggcgcctcgcgcgtcctctacggcaac cgcggcagcaaccgcgcttcgcgggcggagctgctgcgcctggagccggaagacccggcc cacaaaccgccctccccccacgacctcgtatacttcgagaaatcgcccaacttctgcacg tacagcggacgcctgggtacagcgggcacggcagggcgcgcctgtaacagctcgtcgccc gcgctggacggctgcgagctgctctgctgcggcaggggccaccgcacgcgcacgcagcgc gtcaccgagcgctgtaactgcaccttccactggtgctgccacgtcagctgccgcaactgc acgcacacgcgcgtactgcacgagtgtctgtga

Rhinopithecus roxellana (golden snub-nosed monkey): 104679730 Help Entry 104679730         CDS       T03989                                  Gene name WNT10B Definition (RefSeq) protein Wnt-10b   KO K01357   wingless-type MMTV integration site family, member 10 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104679730 (WNT10B)    04390 Hippo signaling pathway     104679730 (WNT10B)    04150 mTOR signaling pathway     104679730 (WNT10B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104679730 (WNT10B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104679730 (WNT10B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104679730 (WNT10B)    05205 Proteoglycans in cancer     104679730 (WNT10B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104679730 (WNT10B)    05226 Gastric cancer     104679730 (WNT10B)    05217 Basal cell carcinoma     104679730 (WNT10B)    05224 Breast cancer     104679730 (WNT10B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104679730 (WNT10B)    05022 Pathways of neurodegeneration - multiple diseases     104679730 (WNT10B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104679730 (WNT10B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104679730 (WNT10B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104679730 (WNT10B) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104679730 (WNT10B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104679730 NCBI-ProteinID:  XP_010383726 UniProt:  A0A2K6RSD6 LinkDB All DBs Position 10 AA seq 389 aa AA seqDB search MPEEPRPRPPPSGLAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG LCLRNPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSP GPGSGSSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR PRRLSGELVYFEKSPDFCERDPTMGSPGTRGRACNKTSHLLDGCGSLCCGRGHNVLRQTR VERCHCRFHWCCYVLCDECKVTEWVNVCK NT seq 1170 nt NT seq  +upstreamnt  +downstreamnt atgccggaggagccccggccgcggcctccgccctcgggcctcgcgggtctcctgttcctg gcgttgtgcagtcgggctctaagcaatgagattctgggcctgaagttgcctggcgaaccg ccgctgacggccaacaccgtgtgcttgacgctgtccggcctgagcaagcggcagctaggc ctgtgcttgcgcaaccccgacgtgacggcgtcggcgcttcagggtctgcacatcgcggtc cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcagcgctcgagggcggt ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgagaaagtgctttttcc ttctccatgctggctgctggggtcatgcacgcagtagccactgcctgcagcctgggcaag ctggtgagctgtggctgtggctggaagggcagtggtgagcaggatcggctgagggccaaa ctgctgcagctgcaggcattgtcccgaggcaagagtttcccccactctctgcccagccct ggccctggctcaggctccagccctggcccccaggacacatgggaatggggtggctgtaac catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc cgggacatccaggcacgaatgcgaatccacaacaacagggtagggcgccaggtggtaact gaaaacctgaagcggaaatgcaagtgtcatggcacgtcaggcagctgccagttcaagaca tgctggagggcggccccagagttccgggcagtgggggcggcgttgagggagcggctgggc cgggccatcttcatcgatacccacaaccgcaattctggagccttccagccccgtctgcgt cctcgtcgcctctcaggagagctggtctactttgagaagtctcctgacttctgtgagcga gaccccactatgggctccccagggacaaggggccgggcctgcaacaagaccagccacctg ttggatggctgtggcagcctgtgctgtggccgtgggcacaacgtgctccggcagacacga gttgagcgctgccattgccgcttccactggtgctgctatgtgctgtgtgatgagtgcaag gttacagagtgggtgaatgtgtgtaagtaa

Rhinopithecus roxellana (golden snub-nosed monkey): 104681717 Help Entry 104681717         CDS       T03989                                  Gene name WNT8A Definition (RefSeq) protein Wnt-8a isoform X1   KO K00714   wingless-type MMTV integration site family, member 8 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104681717 (WNT8A)    04390 Hippo signaling pathway     104681717 (WNT8A)    04150 mTOR signaling pathway     104681717 (WNT8A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104681717 (WNT8A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104681717 (WNT8A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104681717 (WNT8A)    05205 Proteoglycans in cancer     104681717 (WNT8A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104681717 (WNT8A)    05226 Gastric cancer     104681717 (WNT8A)    05217 Basal cell carcinoma     104681717 (WNT8A)    05224 Breast cancer     104681717 (WNT8A)   09164 Neurodegenerative disease    05010 Alzheimer disease     104681717 (WNT8A)    05022 Pathways of neurodegeneration - multiple diseases     104681717 (WNT8A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104681717 (WNT8A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104681717 (WNT8A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104681717 (WNT8A) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104681717 (WNT8A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104681717 NCBI-ProteinID:  XP_010386378 LinkDB All DBs Position 3 AA seq 355 aa AA seqDB search MGSLSMLWAAVGICCAALSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDGSKNG KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDQALKIEMDKRQLRAGNSAEGHWAPAEA FLPSAEAELIFLEESPDYCTCNSSLGIYGTEGRECLQNSHNTSRWERRSCGRLCTECGLQ VEERKTEVISSCNCKFQWCCKVKCDQCRHVVSKYYCTRSSGSAQSLRRVWFGVHI NT seq 1068 nt NT seq  +upstreamnt  +downstreamnt atggggagcctgtctatgctctgggcagctgtgggcatatgctgtgctgcactcagcgcc tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctacctgacctacacg actagcgtggccttgggtgcccagagtggcatcgaggaatgcaagttccagtttgcttgg gaacgctggaactgccctgaaaatgctcttcagctctctacccacaataggctgagaagt gccaccagagagacttccttcatacatgctatcagctctgctggagtcatgtacaccatc accaagaactgtagcatgggtgacttcgaaaactgtggctgtgatgggtcaaaaaatgga aaaacaggaggccatggctggatctggggaggctgcagtgacaatgtggaatttggggaa aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg aatcttcacaacaacagggccggcagactggcagtgagagccaccatgaaaaggacctgc aaatgtcatggcatctctggaagctgcagcatacagacgtgctggctgcagctggctgac ttccgggagatgggagactacctaaaggccaagtatgaccaggcgctgaaaattgaaatg gataagcggcagctgagagctgggaacagcgccgagggccactgggcgcccgctgaggcc ttccttcctagtgcagaggcggaactgatctttttagaggaatcaccagattactgtacc tgcaattccagcctgggcatctatggcacagagggtcgtgagtgcctacagaacagccac aacacatccaggtgggagcgacgtagctgtgggcgcctgtgcactgaatgtgggctgcag gtggaagagaggaaaactgaggtcataagtagctgtaactgcaaattccagtggtgctgt aaggtcaagtgtgaccagtgtaggcatgtggtgagcaagtattactgcacacgctcctca ggcagtgcccagtccctgaggagagtttggtttggggtccatatctag

Rhinopithecus roxellana (golden snub-nosed monkey): 104682399 Help Entry 104682399         CDS       T03989                                  Gene name WNT3 Definition (RefSeq) proto-oncogene Wnt-3   KO K00312   wingless-type MMTV integration site family, member 3 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05206   MicroRNAs in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104682399 (WNT3)    04390 Hippo signaling pathway     104682399 (WNT3)    04150 mTOR signaling pathway     104682399 (WNT3)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104682399 (WNT3)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104682399 (WNT3)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104682399 (WNT3)    05206 MicroRNAs in cancer     104682399 (WNT3)    05205 Proteoglycans in cancer     104682399 (WNT3)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104682399 (WNT3)    05226 Gastric cancer     104682399 (WNT3)    05217 Basal cell carcinoma     104682399 (WNT3)    05224 Breast cancer     104682399 (WNT3)   09164 Neurodegenerative disease    05010 Alzheimer disease     104682399 (WNT3)    05022 Pathways of neurodegeneration - multiple diseases     104682399 (WNT3)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104682399 (WNT3)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104682399 (WNT3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104682399 (WNT3) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104682399 (WNT3) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104682399 NCBI-ProteinID:  XP_010387342 UniProt:  A0A2K6QK28 LinkDB All DBs Position 19 AA seq 355 aa AA seqDB search MEPHLLGLLLGLLLGGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS ASEMVVEKHRESRGWVETLRAKYSLFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECIRIYDVHTCK NT seq 1068 nt NT seq  +upstreamnt  +downstreamnt atggagccccacctgctcgggctgctcctcggcctcctgctcggtggcaccagggtcctc gctggctacccaatttggtggtccctggccctgggccagcagtacacatctctgggctca cagcccctgctctgcggctccatcccaggcctggtccccaagcaactgcgcttctgccgc aattacatcgagatcatgcccagcgtggccgagggcgtgaaactgggcatccaggagtgc cagcaccagttccggggccgccgctggaactgcaccaccatagatgacagcctggccatc tttgggcccgtcctcgacaaagccacccgcgagtcggccttcgtgcacgccatcgcctcg gccggcgtggccttcgccgtcacccgctcctgcgccgagggcacctccaccatttgcggc tgtgactcgcatcataaggggccgcctggcgaaggctggaagtggggcggctgcagcgaa gacgctgacttcggggtgttagtgtccagagagttcgcggacgcgcgtgagaacaggccg gacgcacgctcggccatgaacaagcacaacaacgaggcgggccgcacgactatcctggac cacatgcacctcaaatgcaagtgtcacgggctgtcgggcagctgtgaggtgaagacctgc tggtgggcgcagcctgacttccgtgccattggcgacttcctcaaggacaagtatgacagc gcctcggagatggtagtagagaagcaccgtgagtcccgaggctgggtggagaccctccgg gccaagtactcgctcttcaagccgcccaccgagagggacctggtctactacgagaactcc cccaacttttgtgagcccaacccagagacaggttcttttggcacaagggaccggacttgc aatgtcacctcccatggcattgatggctgcgatctgctctgctgtggccgtggccacaac acgaggacggagaagcggaaggaaaaatgccactgcatcttccactggtgctgctacgtc agctgccaggagtgtattcgcatctacgatgtgcacacctgcaagtag

Rhinopithecus roxellana (golden snub-nosed monkey): 104682400 Help Entry 104682400         CDS       T03989                                  Gene name WNT9B Definition (RefSeq) protein Wnt-9b   KO K01064   wingless-type MMTV integration site family, member 9 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104682400 (WNT9B)    04390 Hippo signaling pathway     104682400 (WNT9B)    04150 mTOR signaling pathway     104682400 (WNT9B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104682400 (WNT9B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104682400 (WNT9B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104682400 (WNT9B)    05205 Proteoglycans in cancer     104682400 (WNT9B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104682400 (WNT9B)    05226 Gastric cancer     104682400 (WNT9B)    05217 Basal cell carcinoma     104682400 (WNT9B)    05224 Breast cancer     104682400 (WNT9B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104682400 (WNT9B)    05022 Pathways of neurodegeneration - multiple diseases     104682400 (WNT9B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104682400 (WNT9B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104682400 (WNT9B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104682400 (WNT9B) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104682400 (WNT9B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104682400 NCBI-ProteinID:  XP_010387343 UniProt:  A0A2K6PMR5 LinkDB All DBs Position 19 AA seq 357 aa AA seqDB search MRPQPALALAGLCLLALPAAAASYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLLKL SRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFLY AVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGSK RGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLKL RYDSAVKVSSATNEALGRLELWAPSRQGSPTKGLAPRSGDLVYMEDSPSFCRPSKYSPGT AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH NT seq 1074 nt NT seq  +upstreamnt  +downstreamnt atgcgcccccagcccgcgctggccctggccgggctctgcctgctggcgctgcccgccgcc gccgcctcctacttcggcctgactgggcgggaggtcctgacgcccttcccaggactgggc actgcggcggccccggcacagggcggggcccacctgaagcagtgcgacctgctgaagctg tcccggcggcagaagcagctctgccggagggagcctggcctggctgagaccctgcgggac gctgcgcacctcggcctgcttgagtgccagttccagttccggcatgagcgctggaactgt agcctggagggcaggacgggcctgctcaagagaggcttcaaagagacagctttcctgtac gcggtgtcctctgccgccctaacccacaccctggcccgggcctgcagcgctgggcgcatg gagcgctgcacctgtgatgactctccggggctggagagccggcaggcctggcagtggggc gtgtgtggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtccaaa agaggaaacaaggacctgcgggcacgggcagacgcccacaacacccacgtgggcatcaag gctgtaaagagtggcctcaggacgacgtgtaagtgccacggcgtgtcaggctcctgtgcc gtgcgcacctgctggaagcagctctccccgttccgtgagacgggccaagtgctaaaactg cgctatgactcggctgtcaaggtgtccagtgccaccaatgaggccttgggccgcctagag ctgtgggccccttccaggcagggcagccccaccaaaggcctggccccgaggtctggggac ctggtctacatggaggactcgcccagcttctgccggcccagcaagtactcgcctggcacg gcaggtagggtatgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctat gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctat gtggagtgccagcaatgtgtgcaggaggagcttgtgtacacctgcaagcactag

Rhinopithecus roxellana (golden snub-nosed monkey): 104682628 Help Entry 104682628         CDS       T03989                                  Gene name WNT2 Definition (RefSeq) protein Wnt-2   KO K00182   wingless-type MMTV integration site family, member 2 Organism rro  Rhinopithecus roxellana (golden snub-nosed monkey) Pathway rro04150   mTOR signaling pathway rro04310   Wnt signaling pathway rro04390   Hippo signaling pathway rro04550   Signaling pathways regulating pluripotency of stem cells rro04916   Melanogenesis rro04934   Cushing syndrome rro05010   Alzheimer disease rro05022   Pathways of neurodegeneration - multiple diseases rro05165   Human papillomavirus infection rro05200   Pathways in cancer rro05205   Proteoglycans in cancer rro05217   Basal cell carcinoma rro05224   Breast cancer rro05225   Hepatocellular carcinoma rro05226   Gastric cancer Brite KEGG Orthology (KO) [BR:rro00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104682628 (WNT2)    04390 Hippo signaling pathway     104682628 (WNT2)    04150 mTOR signaling pathway     104682628 (WNT2)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104682628 (WNT2)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104682628 (WNT2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104682628 (WNT2)    05205 Proteoglycans in cancer     104682628 (WNT2)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104682628 (WNT2)    05226 Gastric cancer     104682628 (WNT2)    05217 Basal cell carcinoma     104682628 (WNT2)    05224 Breast cancer     104682628 (WNT2)   09164 Neurodegenerative disease    05010 Alzheimer disease     104682628 (WNT2)    05022 Pathways of neurodegeneration - multiple diseases     104682628 (WNT2)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104682628 (WNT2)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104682628 (WNT2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:rro00536]     104682628 (WNT2) Glycosaminoglycan binding proteins [BR:rro00536]  Heparan sulfate / Heparin   Morphogens    104682628 (WNT2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104682628 NCBI-ProteinID:  XP_010387638 UniProt:  A0A2K6NI98 LinkDB All DBs Position 6 AA seq 360 aa AA seqDB search MNAPLGGIWLWLPLLLTWLTPEVNSSWWYMRATGGSSRVMCDNVPGLVSSQRQLCHRHPD VMRAISQGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV FAITRACSQGEVKSCSCDPKKMGSAKDSKGIFDWGGCSDNIDYGIKFARAFVDAKERKGK DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG AIQVVMNQDGTGFTVANERFKKPTKNDLVYFENSPDYCVRDREAGSLGTAGRVCNLTSRG MDSCEVMCCGRGYDTSHVTRMTKCGCKFHWCCAVRCQDCLEALDVHTCKAPKNADWTTPT NT seq 1083 nt NT seq  +upstreamnt  +downstreamnt atgaacgcccctctcggtggaatctggctctggctccctctgctcttgacctggctcacc cccgaggtcaactcttcatggtggtacatgagagctacaggtggctcctccagggtgatg tgcgataatgtgccaggcctggtgagcagccagcggcagctgtgtcaccgacatccagat gtgatgcgtgccattagccagggcgtggccgagtggaccgcggaatgccagcaccagttc cgccagcaccgctggaattgcaacactctggacagggatcacagcctctttggcagggtc ctactccgaagtagtcgggaatctgcctttgtttatgccatctcctcagctggagttgta tttgccatcaccagggcctgtagccaaggagaagtaaaatcttgttcctgtgatccaaag aagatgggaagcgccaaggacagcaagggcatttttgattggggtggctgcagtgataac attgactatgggatcaaatttgcccgtgcattcgtggatgccaaggaaaggaaaggaaag gatgccagagccctgatgaatcttcataacaacagagctggcaggaaggctgtaaagcga ttcttgaaacaagagtgcaaatgccatggggtgagcggctcgtgtactctaaggacatgc tggctggccatggccgacttcaggaaaacgggcgattatctctggaggaagtacaatggg gccatccaggtggtcatgaaccaggatggcacaggtttcactgtggctaacgagaggttt aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactactgtgtcagg gaccgagaggcaggctccctgggtacagcaggccgagtgtgcaacctgacttcccggggc atggacagctgcgaagtcatgtgctgtgggagaggctacgacacctcccatgtcacccgg atgaccaagtgtggatgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg gaggccctggacgtgcacacatgcaaggcccccaagaacgctgactggacaacccccaca tga

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