Nannospalax galili (Upper Galilee mountains blind mole rat): 103724772 Help Entry 103724772         CDS       T03372                                  Gene name Wnt3 Definition (RefSeq) Wnt family member 3   KO K00312   wingless-type MMTV integration site family, member 3 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05206   MicroRNAs in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103724772 (Wnt3)    04390 Hippo signaling pathway     103724772 (Wnt3)    04150 mTOR signaling pathway     103724772 (Wnt3)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103724772 (Wnt3)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103724772 (Wnt3)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103724772 (Wnt3)    05206 MicroRNAs in cancer     103724772 (Wnt3)    05205 Proteoglycans in cancer     103724772 (Wnt3)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103724772 (Wnt3)    05226 Gastric cancer     103724772 (Wnt3)    05217 Basal cell carcinoma     103724772 (Wnt3)    05224 Breast cancer     103724772 (Wnt3)   09164 Neurodegenerative disease    05010 Alzheimer disease     103724772 (Wnt3)    05022 Pathways of neurodegeneration - multiple diseases     103724772 (Wnt3)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103724772 (Wnt3)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103724772 (Wnt3)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103724772 (Wnt3) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103724772 (Wnt3) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103724772 NCBI-ProteinID:  XP_008820137 LinkDB All DBs Position Un AA seq 355 aa AA seqDB search MEPHLLGLLLGLLLGGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECIRIYDVHTCK NT seq 1068 nt NT seq  +upstreamnt  +downstreamnt atggagccccacctgctcgggctgctactcggcctcctgctcggtggcaccagggtcctc gccggctacccaatttggtggtccctggccctgggccagcagtacacatctttgggctcc cagcccctgctctgcggctctatcccaggcctggtccccaagcaactgcgcttctgccgc aattacatcgaaatcatgcccagtgtggcagaaggcgtgaagctgggcatccaggagtgc cagcaccagttccgaggccgccgctggaactgcaccaccatagatgacagcctggccatc tttggacctgttctggacaaagccacccgcgagtcggccttcgtgcacgccatcgcctcg gctggcgtagctttcgcggtcacgcgttcctgtgccgagggcacctccaccatctgcggc tgtgactctcatcataaggggccacctggtgaaggctggaagtggggcggctgcagcgag gacgctgacttcggggtgctggtgtcccgggagtttgcagacgcacgtgagaacaggcca gatgcgcgctcggccatgaacaagcacaacaatgaggcaggccgcacgaccatcctggac cacatgcacctcaagtgcaagtgccatgggctgtcaggcagctgtgaggttaagacctgc tggtgggcccagcccgacttccgcgccattggtgacttcctcaaggacaaatatgacagc gcctccgagatggttgtggagaagcaccgggaatcccggggctgggtggagacgctccgg gccaagtatgcactctttaagccacccactgagagggacctggtgtactatgagaactcc cccaacttttgtgagcccaacccagagacaggctcctttggcaccagggaccggacttgc aatgtcacctcccatggcatcgatggttgcgatctgctctgctgtggccgtggccacaac acgaggaccgagaagcggaaggagaagtgtcattgcatcttccactggtgctgctacgtc agctgccaggaatgcatccgcatctatgatgtgcacacctgcaagtag

Nannospalax galili (Upper Galilee mountains blind mole rat): 103724773 Help Entry 103724773         CDS       T03372                                  Gene name Wnt9b Definition (RefSeq) Wnt family member 9B   KO K01064   wingless-type MMTV integration site family, member 9 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103724773 (Wnt9b)    04390 Hippo signaling pathway     103724773 (Wnt9b)    04150 mTOR signaling pathway     103724773 (Wnt9b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103724773 (Wnt9b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103724773 (Wnt9b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103724773 (Wnt9b)    05205 Proteoglycans in cancer     103724773 (Wnt9b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103724773 (Wnt9b)    05226 Gastric cancer     103724773 (Wnt9b)    05217 Basal cell carcinoma     103724773 (Wnt9b)    05224 Breast cancer     103724773 (Wnt9b)   09164 Neurodegenerative disease    05010 Alzheimer disease     103724773 (Wnt9b)    05022 Pathways of neurodegeneration - multiple diseases     103724773 (Wnt9b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103724773 (Wnt9b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103724773 (Wnt9b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103724773 (Wnt9b) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103724773 (Wnt9b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103724773 NCBI-ProteinID:  XP_008820139 LinkDB All DBs Position Un AA seq 359 aa AA seqDB search MRPAPTLALVALCLLALPVAAAAAAYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLL KLSRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRQERWNCSLEGRTGLLKRGFKETAF LYAVSAAALTHALARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLG PKRGSKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVL KLRYDTAVKVSSATNEALDRLELWTPAKPGGPAKGLPPRPGDLVYMEDSPSFCRPSKYSP GTAGRVCSRDASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCAQQELVYTCKR NT seq 1080 nt NT seq  +upstreamnt  +downstreamnt atgcgccccgcgcccacgctggccctggtcgcgctctgcctgctagcgctgcccgtcgcc gccgccgccgccgcctacttcggcctaactgggcgcgaggtcctgacgcccttcccaggc ctgggcacagcagcagctccggcacagggtggtgcccacctgaagcagtgtgacctgctg aagctatcccgtcgccagaagcagctctgccggagggagcctggcctggctgaaaccctg agggatgctgcacacctcggcctgctggaatgccagttccagttccgacaggagcggtgg aactgcagcctggaggggaggactggcctgctcaagagaggcttcaaggagacagctttc ctgtacgcagtgtctgcggccgccctcacgcatgcactagcccgggcttgcagtgccggt cgcatggagcgctgtacctgtgacgactcccctggcctggagagtcggcaggcctggcag tggggtgtgtgtggtgacaacctcaagtacagcaccaagtttctgagtaacttcctgggg cccaagagaggaagcaaagacctacgggctcgagctgatgcccacaacacccatgtaggc atcaaggccgtaaagagtggcctcaggactacctgtaagtgccatggagtgtcaggctcc tgtgctgtgcgtacctgctggaagcagctctccccattccgagagacaggccaggtgctg aagctgcgctatgacacagctgtcaaggtatctagtgccaccaatgaggccttagatcgc ctggagctatggacacctgccaagccaggtggcccggctaagggcctgccaccccggcca ggggacctggtctacatggaggattctcccagcttctgccggcccagcaagtactctcct ggcacagctggaagggtgtgctcccgtgatgccagctgcagcagcctatgctgtgggcgg ggctatgacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgc tgttacgtggagtgccagcagtgtgcacagcaggagcttgtgtatacctgtaagcgctaa

Nannospalax galili (Upper Galilee mountains blind mole rat): 103727729 Help Entry 103727729         CDS       T03372                                  Gene name Wnt6 Definition (RefSeq) Wnt family member 6   KO K00445   wingless-type MMTV integration site family, member 6 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103727729 (Wnt6)    04390 Hippo signaling pathway     103727729 (Wnt6)    04150 mTOR signaling pathway     103727729 (Wnt6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103727729 (Wnt6)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103727729 (Wnt6)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103727729 (Wnt6)    05205 Proteoglycans in cancer     103727729 (Wnt6)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103727729 (Wnt6)    05226 Gastric cancer     103727729 (Wnt6)    05217 Basal cell carcinoma     103727729 (Wnt6)    05224 Breast cancer     103727729 (Wnt6)   09164 Neurodegenerative disease    05010 Alzheimer disease     103727729 (Wnt6)    05022 Pathways of neurodegeneration - multiple diseases     103727729 (Wnt6)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103727729 (Wnt6)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103727729 (Wnt6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103727729 (Wnt6) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103727729 (Wnt6) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103727729 NCBI-ProteinID:  XP_008823958 LinkDB All DBs Position Un AA seq 365 aa AA seqDB search MLPPVPSRLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV TQACSMGELLQCGCQAPRGRAPPRPSGLLGTPGPPGPAGSPDASAAWEWGGCGDDVDFGD EKSRLFMDAQHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE LSLCL NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atgctgccgccggtgccctcccgcctcgggctgctgctgctgctgctcctgtgtccggcg cacgtcggaggcctgtggtgggccgtgggcagccccttagtcatggaccctaccagtatc tgcagaaaggcccggaggctggcaggacggcaggctgagttgtgccaggcagagccggaa gtggtggcagagctagcccggggagcgcggctcggggtgcgagaatgccagttccagttc cgctttcgtcgctggaactgctccagccacagcaaggcctttgggcgcatcctgcagcag gacatcagagagacagccttcgtgtttgcaatcactgcagctggcgccagccacgctgtc acgcaggcctgttccatgggcgagcttctgcagtgcggttgccaagcaccacgcgggcgg gcaccccctaggccctccggtctgctgggcaccccaggacccccaggcccagcaggctcc ccagacgccagcgctgcttgggaatggggaggctgcggcgacgacgtggacttcggggac gagaaatcaaggctctttatggatgcgcagcacaagcgcggacgcggagacatccgtgcg ttggtgcaattgcacaacaatgaggcaggcaggctggcggtgcggagccacacacgcaca gaatgcaagtgccatgggctttcgggttcgtgcgcgctgcgcacctgctggcagaagctg cccccgttccgagaggtgggggcgcggctgctggagcgcttccacggcgcctcgcgtgtc atgggcactaacgacggcaaagccctgctgcccgcggtccgcacgctcaagccgccgggc cgagctgatctcctttatgccgctgactcgccggacttctgcgcccctaataggcgcacc ggctctcctggcacccgtggccgagcctgcaacagcagtgccccggacctcagcggctgc gacctgttgtgctgcggtcgtggacaccgccaggagagcgtacagctcgaggagaattgc ctgtgccgcttccactggtgctgtgtggtgcagtgccaccgctgccgggtgcgcaaggag ctcagtctgtgcctctga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103727730 Help Entry 103727730         CDS       T03372                                  Gene name Wnt10a Definition (RefSeq) Wnt family member 10A   KO K01357   wingless-type MMTV integration site family, member 10 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103727730 (Wnt10a)    04390 Hippo signaling pathway     103727730 (Wnt10a)    04150 mTOR signaling pathway     103727730 (Wnt10a)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103727730 (Wnt10a)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103727730 (Wnt10a)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103727730 (Wnt10a)    05205 Proteoglycans in cancer     103727730 (Wnt10a)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103727730 (Wnt10a)    05226 Gastric cancer     103727730 (Wnt10a)    05217 Basal cell carcinoma     103727730 (Wnt10a)    05224 Breast cancer     103727730 (Wnt10a)   09164 Neurodegenerative disease    05010 Alzheimer disease     103727730 (Wnt10a)    05022 Pathways of neurodegeneration - multiple diseases     103727730 (Wnt10a)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103727730 (Wnt10a)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103727730 (Wnt10a)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103727730 (Wnt10a) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103727730 (Wnt10a) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103727730 NCBI-ProteinID:  XP_008823959 LinkDB All DBs Position Un AA seq 416 aa AA seqDB search MGSAYPRPWLRLPPRPQPRPELWALLFFLLLLAAAVPRSAPNDILGLRVPEPVLNANTVC LTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKIPYESP IFSRGFRESAFAYAIAAAGVVHAVSNACALGKLQACGCDASRRGDEEAFRRKLHRLQVDA LQRGKGLSHGVPEHPALPPASPGLQDSWEWGGCSPDVGFGERFSKDFLDSREPHRDIHAR MRLHNNRVGRQAVMENMRRKCKCHGTSGSCQLKTCWQVTPEFRAVGALLRNRFHRATLIR PHNRNGGQLEPGPAGVPSPAPGTPVPRRRANPSDLVYFEKSPDFCEREPRLDSAGTVGRL CNKSSAGPDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK NT seq 1251 nt NT seq  +upstreamnt  +downstreamnt atgggcagcgcctaccctcgcccctggctgcggctcccaccccggccccagccgcggcct gagctctgggcgctcctgttctttctactgctgctggctgccgctgtgcccaggtcagca cccaatgacatcctgggccttcgagtaccagagcctgtgctcaatgccaacacagtgtgc ctgacattgcccggcctgagcaggcggcagatggaggtgtgtgtgcgtcaccctgacgtg gccgcttctgccatccagggcatccagatcgccatccatgagtgccaacaccagttccgg gaccagcgctggaactgctctagcctggagactcgaaacaaaatcccctacgaaagtccc atcttcagcagaggttttcgagagagtgcttttgcctatgccatcgctgctgcaggggtg gtgcacgcagtgtccaacgcgtgcgccctgggtaaactgcaggcctgcggttgcgacgcc tccaggcgtggggacgaagaggccttccgtcggaagctgcaccgcctgcaagtagacgcc ctgcaacgcgggaagggcctgagccacggggtcccggaacaccctgccctgccccctgcc agtccaggcctgcaggactcctgggaatggggcggctgcagtcctgacgtgggcttcgga gaacgcttctctaaggactttctggactcccgggagcctcacagagacatccacgctcgc atgagactccacaataaccgagtgggccgacaggcggtgatggagaacatgcggcgaaag tgcaagtgccatggcacgtcaggtagctgccagctcaagacgtgctggcaggtgacgcct gaattccgcgcggtgggggcgctgctgcgcaaccgcttccaccgcgccacgctcatccgg ccgcacaaccgcaacggaggccagctggagcccggccctgcgggggtaccctcgccagcc ccgggcactcccgtgccgcgccgccgggccaacccctccgacttggtatacttcgagaaa tctcccgacttctgcgagcgcgagccgcgcctggactcggcgggcactgtgggccgcctt tgcaacaagagcagcgcgggcccggatggctgcggcagcatgtgctgcggccggggccac aacatcctgcgccagacacgaagcgagcgctgccactgccgcttccactggtgctgcttc gtggtctgcgaagaatgccgcatcaccgagtgggtcagcgtctgcaagtga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103730373 Help Entry 103730373         CDS       T03372                                  Gene name Wnt7a Definition (RefSeq) Wnt family member 7A   KO K00572   wingless-type MMTV integration site family, member 7 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103730373 (Wnt7a)    04390 Hippo signaling pathway     103730373 (Wnt7a)    04150 mTOR signaling pathway     103730373 (Wnt7a)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103730373 (Wnt7a)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103730373 (Wnt7a)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103730373 (Wnt7a)    05205 Proteoglycans in cancer     103730373 (Wnt7a)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103730373 (Wnt7a)    05226 Gastric cancer     103730373 (Wnt7a)    05217 Basal cell carcinoma     103730373 (Wnt7a)    05224 Breast cancer     103730373 (Wnt7a)   09164 Neurodegenerative disease    05010 Alzheimer disease     103730373 (Wnt7a)    05022 Pathways of neurodegeneration - multiple diseases     103730373 (Wnt7a)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103730373 (Wnt7a)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103730373 (Wnt7a)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103730373 (Wnt7a) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103730373 (Wnt7a) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt COG6 Motif Other DBs NCBI-GeneID:  103730373 NCBI-ProteinID:  XP_008826816 LinkDB All DBs Position Un AA seq 349 aa AA seqDB search MTRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgacccggaaagcgcggcgctgccttggccacctctttctcagcctgggcatggtctac cttcggatcggtggcttctcttctgtggtagctctgggtgcgagcatcatctgtaacaag atcccaggcctggctcccagacagcgggcaatctgccagagccggcccgacgccatcatc gtcataggagaaggctcccaaatgggcctcgatgagtgtcagtttcagttccgaaatggt cgttggaactgctcagcactgggggagcgcacagtcttcgggaaggagctcaaagtgggg agccgggaggctgccttcacctatgccatcattgctgcgggtgtggcccacgccattaca gctgcctgcacccagggcaatctgagtgactgtggctgcgacaaggagaagcaaggccag taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc ggcttcgccaaggtctttgtggatgcccgggaaatcaagcagaatgcccggactctcatg aacttacacaataatgaggcgggccgaaagatcctggaggagaacatgaagctggagtgt aagtgtcatggtgtgtcaggctcctgtaccaccaagacatgctggaccacactgccacaa ttccgagagctgggctacgtgctcaaggacaaatacaacgaggccgtccatgtggaaccc gtgcgtgccagccgcaataagcggcccaccttcctaaagatcaagaagcccctgtcttac cgcaagcccatggacacagacctggtatatatcgagaagtcacccaattactgtgaagag gacccagtgacaggcagcgtgggtacacagggccgtgcctgcaataagacagccccacag gccagcggttgtgacctcatgtgctgtggccgtggctacaacacacaccagtatgcccgc gtgtggcaatgcaactgcaagttccactggtgctgctatgtcaagtgcaacacgtgcagt gagcgcaccgagatgtacacgtgcaagtaa

Nannospalax galili (Upper Galilee mountains blind mole rat): 103730604 Help Entry 103730604         CDS       T03372                                  Gene name Wnt16 Definition (RefSeq) Wnt family member 16   KO K01558   wingless-type MMTV integration site family, member 16 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05202   Transcriptional misregulation in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103730604 (Wnt16)    04390 Hippo signaling pathway     103730604 (Wnt16)    04150 mTOR signaling pathway     103730604 (Wnt16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103730604 (Wnt16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103730604 (Wnt16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103730604 (Wnt16)    05202 Transcriptional misregulation in cancer     103730604 (Wnt16)    05205 Proteoglycans in cancer     103730604 (Wnt16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103730604 (Wnt16)    05226 Gastric cancer     103730604 (Wnt16)    05217 Basal cell carcinoma     103730604 (Wnt16)    05224 Breast cancer     103730604 (Wnt16)   09164 Neurodegenerative disease    05010 Alzheimer disease     103730604 (Wnt16)    05022 Pathways of neurodegeneration - multiple diseases     103730604 (Wnt16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103730604 (Wnt16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103730604 (Wnt16)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103730604 (Wnt16) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103730604 (Wnt16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103730604 NCBI-ProteinID:  XP_008827104 LinkDB All DBs Position Un AA seq 364 aa AA seqDB search MDRAALLALPRLCALWAAVLALFPCGAQGNWMWLGIASFGVPEKLGCASLPLNSRQKELC KRKPYLLPSIREGARLGIQECRSQFRHERWNCKVATPAAAPPDTGPLFGYELSSGTKETA FIYAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRK FLDFPIRNTTEKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSS FEKIGHFLKDKYENSIQISDKTKRKVRRREKDQRKTPIRKDDLLYVHKSPNYCMEDKKLG IPGTQGRECNRTSGGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRSCESMTDV HTCK NT seq 1095 nt NT seq  +upstreamnt  +downstreamnt atggacagagctgcgctcctggcactgcctcgcttgtgcgcgctgtgggctgcggtgctc gcgctgttcccttgcggagcccagggcaactggatgtggttgggcatcgcctccttcggg gttcctgagaagctgggctgcgccagcttgccactaaacagccgccagaaggagctgtgc aagaggaaaccttacctgctgcccagcatccgcgagggcgccaggctgggcattcaggag tgcaggagccagttccgacacgagagatggaactgcaaggtcgccacacccgccgcagcc ccgccggacaccggtcccctctttggctatgagttgagcagtggcaccaaggagacagca ttcatttatgctgtgatggctgcaggcctggtgcactctgtgactaggtcgtgcagtgca ggaaacatgacagaatgctcctgcgataccaccttacagaatggtggctcagcaagtgaa ggctggcattgggggggatgctctgatgatgtccagtacggcatgtggttcagcagaaag ttcctagatttccccatcagaaataccacagaaaaagaaagcaaagtattgctggccatg aacctacacaacaatgaagctggacggcaggctgtagccaagttgatgtcggtggactgc cgctgccatggggtttcgggctcttgtgccgtgaaaacctgctggaaaaccatgtcttct tttgaaaagattggccattttttaaaagataaatatgaaaacagcatccagatatcggac aaaaccaagaggaaagtgcgcaggagagaaaaagatcagaggaagacacccatccgcaag gatgacctactgtatgttcataagtctcccaactactgtatggaggacaaaaaactgggt atcccagggacacaaggcagagagtgcaaccgcacatcaggaggcgcagacgggtgcaac ctcctctgctgtggccgtggctacaacacccatgtggtcagacacgtggagaggtgtgag tgtaagtttatctggtgctgctacgttcgctgcaggagctgtgaaagcatgaccgatgtc catacttgtaagtaa

Nannospalax galili (Upper Galilee mountains blind mole rat): 103734912 Help Entry 103734912         CDS       T03372                                  Gene name Wnt2b Definition (RefSeq) Wnt family member 2B   KO K00182   wingless-type MMTV integration site family, member 2 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103734912 (Wnt2b)    04390 Hippo signaling pathway     103734912 (Wnt2b)    04150 mTOR signaling pathway     103734912 (Wnt2b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103734912 (Wnt2b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103734912 (Wnt2b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103734912 (Wnt2b)    05205 Proteoglycans in cancer     103734912 (Wnt2b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103734912 (Wnt2b)    05226 Gastric cancer     103734912 (Wnt2b)    05217 Basal cell carcinoma     103734912 (Wnt2b)    05224 Breast cancer     103734912 (Wnt2b)   09164 Neurodegenerative disease    05010 Alzheimer disease     103734912 (Wnt2b)    05022 Pathways of neurodegeneration - multiple diseases     103734912 (Wnt2b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103734912 (Wnt2b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103734912 (Wnt2b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103734912 (Wnt2b) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103734912 (Wnt2b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103734912 NCBI-ProteinID:  XP_008832185 LinkDB All DBs Position Un AA seq 393 aa AA seqDB search MLKPRGAEEAAQLASRRARALVPAPAPRPLAPDVSPASARLSLACLLLLLLLTLPARVDT SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD QRGDFDWGGCSDNIHYGIRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT NT seq 1182 nt NT seq  +upstreamnt  +downstreamnt atgctgaagccgcggggtgcggaggaagccgcgcagctcgcctctcggcgcgcccgcgcc ctggtccccgcgccggcgcccagacccttggcccccgacgtgtccccggcttcggcccgt ctgagtcttgcctgcctgttgctgctactactgctgacactgccggcccgtgtagacacg tcctggtggtacataggggcactgggagcccgagtgatctgtgacaacatcccaggtttg gtgagccggcagcggcagctgtgtcagcgttacccagatatcatgcgctccgtgggcgaa ggcgcccgagaatggatccgagagtgtcagcatcagtttcgccatcaccgttggaactgc accacactggaccgggaccacactgtctttggccgggtcatgctcagaagtagccgggag gcagcatttgtatatgccatctcatcagcaggagtggtccacgcaatcactcgggcctgc agccagggtgaactgagtgtgtgcagctgtgacccatatacccgtggtcgacaccatgac caacgaggggactttgattggggtggctgcagtgacaacatccactatggtattcgcttt gctaaggcctttgtggatgccaaggagaagaggctcaaggacgccagggccctcatgaac ttacataacaaccgctgtggtcgtacggctgtgcgaagatttctgaagctggagtgtaag tgtcatggtgtgagtggctcctgtactctgcgaacctgctggcgtgcactctcagacttc cgccgcacaggtgattacctgcgtaggcgctatgatggggctgtgcaggtgacggccacc caggatggtgccaatttcacagcagcccgccaaggctatcgtcgtgccacccgaactgac cttgtctactttgataactctccagactactgtgtcttggacaaggctgcaggttcccta ggtactgcaggtcgtgtctgcagcaagacatctaaaggaacagatggttgtgaaatcatg tgttgcggccgagggtatgacacaactcgagtcacccgtgtcacccagtgtgagtgcaaa ttccactggtgctgtgctgtacggtgcaaggagtgcagaaacactgtggacgtccacact tgcaaggcccccaagaaagcagagtggttggaccagacctga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103735176 Help Entry 103735176         CDS       T03372                                  Gene name Wnt8a Definition (RefSeq) Wnt family member 8A   KO K00714   wingless-type MMTV integration site family, member 8 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103735176 (Wnt8a)    04390 Hippo signaling pathway     103735176 (Wnt8a)    04150 mTOR signaling pathway     103735176 (Wnt8a)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103735176 (Wnt8a)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103735176 (Wnt8a)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103735176 (Wnt8a)    05205 Proteoglycans in cancer     103735176 (Wnt8a)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103735176 (Wnt8a)    05226 Gastric cancer     103735176 (Wnt8a)    05217 Basal cell carcinoma     103735176 (Wnt8a)    05224 Breast cancer     103735176 (Wnt8a)   09164 Neurodegenerative disease    05010 Alzheimer disease     103735176 (Wnt8a)    05022 Pathways of neurodegeneration - multiple diseases     103735176 (Wnt8a)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103735176 (Wnt8a)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103735176 (Wnt8a)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103735176 (Wnt8a) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103735176 (Wnt8a) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103735176 NCBI-ProteinID:  XP_008832546 LinkDB All DBs Position Un AA seq 411 aa AA seqDB search MGDLFMLWVTVGMCYATFSASAWSVNNFLITGPKAYLTYATSAALGAQSGIEECKFQFVW ERWNCPENALQLSTHNRLRGATRETAFIHAISSAGVMHAITKNCSMGDFENCGCDESKKG KTGGRGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRVGRLAARATMKRTC KCHGLSGSCSIQTCWLQLASIREIGDYLKAKYDWALKIEMDKHQLRAGNSAEGHWDPMET FFPGAEAELIFLEESPDYCTRNTSLGIYGTEGRECLQRSHNASRWEQHNCGRLCTECGLQ VEERRTEATSSCNCKFQWCCTVKCDQCRHVVNKYYCRRYLGRARTRGKRGWFGVHIQRNL KSICYIKFQTLSRPAVVLRVRETRIKEFPEKAILGRMRQKPPSPIGRFLEG NT seq 1236 nt NT seq  +upstreamnt  +downstreamnt atgggggacttgtttatgctgtgggtgactgtgggcatgtgctatgccaccttcagtgcc tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctatctgacctatgct accagtgcagccttgggcgctcagagtggcatcgaagaatgtaagttccagtttgtgtgg gaacgctggaactgtcctgaaaatgccctccaactctccacccataacagactgagaggt gccacgagagagactgccttcattcatgccatcagctctgctggagtcatgcacgccatc accaagaactgcagcatgggtgactttgaaaactgtggctgtgatgagtcaaaaaaggga aaaacaggaggccgtggctggatctggggaggctgcagcgacaatgtggaatttggggaa aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg aatcttcacaacaacagggtcggcaggctggcagcgagagccaccatgaaaaggacctgc aaatgtcacggcctgtcagggagctgcagcatccagacatgctggctgcaactggctagc attcgggagataggagactacctaaaggccaagtatgactgggcactgaaaattgagatg gataagcatcagctcagggctggcaacagtgctgagggccactgggatcccatggagacc ttctttcctggtgcagaggccgagttgatcttcttagaggaatctcctgactactgtaca cgcaacaccagcctgggcatctatggcaccgagggtcgcgaatgcctgcagagaagccac aacgcttccaggtgggaacaacacaactgtgggcgcttatgcactgagtgtggtctgcag gtggaagagaggagaactgaggccacaagcagctgtaactgcaagttccagtggtgctgc acagtcaagtgtgatcagtgtaggcacgtggtgaacaagtactactgcagaaggtatcta ggcagagccaggacccggggcaagagaggatggtttggggtgcacatccagaggaacctg aaaagcatttgttacattaagtttcagactctgtccaggccagctgtggtgctgagagtc agggagactagaatcaaagaattccctgaaaaagcaatcttaggcagaatgaggcagaaa ccaccttctcctattgggaggtttttagagggctga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103737375 Help Entry 103737375         CDS       T03372                                  Gene name Wnt2 Definition (RefSeq) Wnt family member 2   KO K00182   wingless-type MMTV integration site family, member 2 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103737375 (Wnt2)    04390 Hippo signaling pathway     103737375 (Wnt2)    04150 mTOR signaling pathway     103737375 (Wnt2)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103737375 (Wnt2)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103737375 (Wnt2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103737375 (Wnt2)    05205 Proteoglycans in cancer     103737375 (Wnt2)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103737375 (Wnt2)    05226 Gastric cancer     103737375 (Wnt2)    05217 Basal cell carcinoma     103737375 (Wnt2)    05224 Breast cancer     103737375 (Wnt2)   09164 Neurodegenerative disease    05010 Alzheimer disease     103737375 (Wnt2)    05022 Pathways of neurodegeneration - multiple diseases     103737375 (Wnt2)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103737375 (Wnt2)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103737375 (Wnt2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103737375 (Wnt2) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103737375 (Wnt2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103737375 NCBI-ProteinID:  XP_008835456 LinkDB All DBs Position Un AA seq 360 aa AA seqDB search MNVPLGGIWLWLPLLLTWLTPEVSSSWWYMRATGGSSRVMCDNVPGLVSRQRQLCHRHPD VMRAIGLGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV FAITRACSQGELKSCSCDPKKKGSAKDSKGTFDWGGCSDNIDYGIKFARAFADAKERKGK DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDREAGSLGTAGRVCNLTSRG MDSCEVMCCGRGYDTSHVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSADWTTPT NT seq 1083 nt NT seq  +upstreamnt  +downstreamnt atgaacgtccctctcggtggaatctggctctggctccctctgctcttgacctggctcacc cctgaggtcagctcttcatggtggtacatgagagctacaggtggctcctccagggtgatg tgtgacaatgtgccaggcctggtgagccgccagcgtcagctgtgccaccgacatccagac gtgatgcgtgccattggcctgggtgtggctgagtggacagcagagtgccaacaccagttc cggcagcaccgctggaactgcaacactctagacagggatcacagcctctttggccgggtc ctcctcagaagtagtcgggaatctgcctttgtttacgccatctcctcagctggagttgta tttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgatccaaag aagaagggaagtgccaaggacagcaagggtacctttgactggggtggctgcagcgacaac attgactatgggatcaaatttgcccgagcgtttgcagatgccaaggaaaggaaagggaag gatgccagagccctgatgaatcttcacaacaacagagccggaaggaaggcagtaaagcga ttcctgaagcaagagtgcaagtgtcatggcgtgagtggctcctgtactctgaggacatgc tggctggccatggccgacttcaggaaaacaggcgattatctctggaggaagtacaacggg gccatccaggttgtcatgaaccaggatggcacaggcttcactgtggcaaataagagattt aagaagccaacgaaaaatgacctcgtgtattttgagaactctccagactactgtatcagg gaccgagaggcaggctccctgggtacagcaggtcgtgtgtgcaacttgacttcccgaggc atggacagctgtgaagtcatgtgctgtgggagaggctatgacacctctcatgtcacccgg atgaccaagtgtgagtgtaaattccactggtgctgtgctgtgcgctgtcaggactgcctg gaggccctggatgtacacacatgcaaggcccccaagagtgccgattggacaacccctaca tga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103739037 Help Entry 103739037         CDS       T03372                                  Gene name Wnt3a Definition (RefSeq) Wnt family member 3A   KO K00312   wingless-type MMTV integration site family, member 3 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05206   MicroRNAs in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103739037 (Wnt3a)    04390 Hippo signaling pathway     103739037 (Wnt3a)    04150 mTOR signaling pathway     103739037 (Wnt3a)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103739037 (Wnt3a)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103739037 (Wnt3a)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103739037 (Wnt3a)    05206 MicroRNAs in cancer     103739037 (Wnt3a)    05205 Proteoglycans in cancer     103739037 (Wnt3a)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103739037 (Wnt3a)    05226 Gastric cancer     103739037 (Wnt3a)    05217 Basal cell carcinoma     103739037 (Wnt3a)    05224 Breast cancer     103739037 (Wnt3a)   09164 Neurodegenerative disease    05010 Alzheimer disease     103739037 (Wnt3a)    05022 Pathways of neurodegeneration - multiple diseases     103739037 (Wnt3a)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103739037 (Wnt3a)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103739037 (Wnt3a)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103739037 (Wnt3a) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103739037 (Wnt3a) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103739037 NCBI-ProteinID:  XP_008837561 LinkDB All DBs Position Un AA seq 352 aa AA seqDB search MATLGYFLVLCSLKQALGSYPIWWSLAVGPQYSSLSTQPILCASIPGLVPKQLRFCRNYV EIMPSVAEGVKAGIQECQHQFRGRRWNCTTVSNSLAIFGPVLDKATRESAFVHAIASAGV AFAVTRSCAEGSAAICGCSSRLQGSPGEGWKWGGCSEDIEFGGMVSREFADARENRPDAR SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRTIGDFLKDKYDSASE MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVS SHGIDGCDLLCCGRGHNARTERRREKCQCVFHWCCYVSCQECTRVYDVHTCK NT seq 1059 nt NT seq  +upstreamnt  +downstreamnt atggctacactcggatacttcttagtgctctgcagcctgaagcaggcactgggcagctac ccgatctggtggtccttggctgtggggccccagtactcctccctgagcacccagcccatc ctctgtgccagtattccgggcctggtgcccaagcagctgcgcttctgcaggaactacgtc gagatcatgcccagtgtggctgagggcgtcaaggccggcattcaggagtgccaacatcag ttccgtggccggcgctggaactgtaccactgtcagcaacagccttgccatctttggcccc gtgctggacaaagccacccgggagtcagccttcgtccacgctatcgcctctgcgggagtg gccttcgcagtgacacgctcctgtgctgagggttctgctgccatctgtgggtgcagtagc cgcctccagggctccccaggcgagggctggaagtggggcggctgtagcgaggacattgaa tttggaggaatggtgtctcgagagtttgcagatgcccgagagaaccgaccagatgcccgc tctgctatgaaccgccataacaatgaggctgggcgtcaggccatcgccagccacatgcac ctcaagtgcaaatgccatgggctgtcaggcagctgcgaggtgaaaacctgctggtggtct cagcctgatttccggaccatcggcgacttcctcaaggacaagtacgacagcgcctccgag atggtggtggagaaacaccgcgagtctcgtggctgggtggagaccctgcggccgcgctac acgtacttcaaggtgcccacagagcgcgacctggtctattacgaggcgtcgcccaacttc tgcgagcccaaccccgagaccggctcctttgggacacgcgaccgcacctgcaacgtgagc tcgcacggcatcgacggctgcgacctgctgtgctgcggccgtggccacaacgcgcgcacc gagcggcgcagggagaagtgccagtgcgtcttccactggtgctgctatgtcagctgtcaa gagtgcacgcgcgtttacgacgtgcacacctgcaagtaa

Nannospalax galili (Upper Galilee mountains blind mole rat): 103739374 Help Entry 103739374         CDS       T03372                                  Gene name Wnt5b Definition (RefSeq) Wnt family member 5B   KO K00444   wingless-type MMTV integration site family, member 5 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04360   Axon guidance ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103739374 (Wnt5b)    04390 Hippo signaling pathway     103739374 (Wnt5b)    04150 mTOR signaling pathway     103739374 (Wnt5b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103739374 (Wnt5b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103739374 (Wnt5b)   09158 Development and regeneration    04360 Axon guidance     103739374 (Wnt5b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103739374 (Wnt5b)    05205 Proteoglycans in cancer     103739374 (Wnt5b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103739374 (Wnt5b)    05226 Gastric cancer     103739374 (Wnt5b)    05217 Basal cell carcinoma     103739374 (Wnt5b)    05224 Breast cancer     103739374 (Wnt5b)   09164 Neurodegenerative disease    05010 Alzheimer disease     103739374 (Wnt5b)    05022 Pathways of neurodegeneration - multiple diseases     103739374 (Wnt5b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103739374 (Wnt5b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103739374 (Wnt5b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103739374 (Wnt5b) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103739374 (Wnt5b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103739374 NCBI-ProteinID:  XP_008837973 LinkDB All DBs Position Un AA seq 372 aa AA seqDB search MLVPGYWDGLRLTMPSLPLLFTAALLSSWAQLLTDASSWWSLAMNPVQRPEMFIIGAQPV CSQLPGLSPGQRKLCQLYQEHMAYIGEGAKMGIRECQHQFRQRRWNCSTVDNTSVFGRVM QIGSRETAFTYAVSAAGVVNAISRACREGELSTCGCSRAVRPKDLPRDWLWGGCGDNVEY GYRFAKEFVDAREREKNFVKGSEEQGRALMNLQNNEAGRRAVYKMADVACKCHGVSGSCS LKTCWLQLAEFRKVGDRLKEKYDGAAAMRITRQGKLELVNSRFNQPTPEDLVYVDPSPDY CLRNETTGSMGTQGRLCNKTSEGMDGCELMCCGRGYDRFKSVQVERCHCKFHWCCFVRCK KCTEIVDQYICK NT seq 1119 nt NT seq  +upstreamnt  +downstreamnt atgttggtcccagggtactgggacgggctgaggctgaccatgcccagcctccctttgctg tttactgcagctctgctctccagctgggcccagctactgactgacgccagttcctggtgg tcactagctatgaacccggtgcagagacctgagatgtttatcatcggtgctcagcctgtg tgcagccagcttcctgggctctccccaggccagagaaagctatgccagttgtatcaggag cacatggcctacatcggggagggagccaagatgggcatcagggagtgccagcaccagttc cgacagaggaggtggaactgcagcaccgtggacaacacatccgtctttggcagagtcatg cagataggcagccgggaaaccgccttcacctatgctgtgagtgctgctggtgtggtgaat gccatcagccgtgcttgccgagagggtgagctgtccacttgtggttgcagccgggccgta aggcccaaggacttgccacgagactggctgtggggtggctgtggggacaacgtggagtac ggctaccgctttgctaaggagtttgtggatgctcgagagcgagagaagaactttgtcaag ggctcagaggagcagggccgagccctcatgaacctacagaacaatgaggctggtcgccgg gctgtgtataagatggctgatgttgcctgcaaatgtcacggggtctcagggtcctgcagc ctcaagacctgctggctccagttggccgagttccgaaaggtgggagaccgtttgaaggag aaatatgatggtgctgccgccatgcgcatcacccgccagggcaagctggagctggttaac agccgctttaaccagcccaccccagaggacctggtctacgtggaccccagccctgattac tgcctgcgcaatgagaccacaggctcgatgggcacccagggacgcctctgcaacaagacc tcagagggcatggatggctgtgagctcatgtgctgtggccgtggctatgaccggtttaag agcgtccaggtggagcgttgccactgcaaattccactggtgctgttttgtcagatgcaaa aagtgcactgagattgttgaccagtacatctgtaaataa

Nannospalax galili (Upper Galilee mountains blind mole rat): 103740409 Help Entry 103740409         CDS       T03372                                  Gene name Wnt9a Definition (RefSeq) Wnt family member 9A   KO K01064   wingless-type MMTV integration site family, member 9 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103740409 (Wnt9a)    04390 Hippo signaling pathway     103740409 (Wnt9a)    04150 mTOR signaling pathway     103740409 (Wnt9a)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103740409 (Wnt9a)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103740409 (Wnt9a)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103740409 (Wnt9a)    05205 Proteoglycans in cancer     103740409 (Wnt9a)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103740409 (Wnt9a)    05226 Gastric cancer     103740409 (Wnt9a)    05217 Basal cell carcinoma     103740409 (Wnt9a)    05224 Breast cancer     103740409 (Wnt9a)   09164 Neurodegenerative disease    05010 Alzheimer disease     103740409 (Wnt9a)    05022 Pathways of neurodegeneration - multiple diseases     103740409 (Wnt9a)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103740409 (Wnt9a)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103740409 (Wnt9a)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103740409 (Wnt9a) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103740409 (Wnt9a) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Clr5 Motif Other DBs NCBI-GeneID:  103740409 NCBI-ProteinID:  XP_008839249 LinkDB All DBs Position Un AA seq 343 aa AA seqDB search MNVHGAMLHLLTGSEPLTILPLTLETEAAAQAHYKACDRLKLERKQRRMCRRDPGVAETL VEAVSMSALECQYQFRFERWNCTLEGRYRASLLKRGFKETAFLYAISSAGLTHALAKACS AGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKDLRARVDFHNNLV GVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVGKHLKHKYETALKVGSTTNEATG EAGAISPPRGRASGSGGGDPLPRTPELVHLDDSPSFCLAGRFSPGTAGRRCHREKNCESI CCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEVYTCKG NT seq 1032 nt NT seq  +upstreamnt  +downstreamnt atgaacgtgcatggggccatgctacacctgctgacaggcagtgagcccctgaccattctt cctctgactctggagaccgaggcagcagcccaggcacactacaaggcctgtgaccggctg aagctggaacgcaagcagcgccgcatgtgccgccgggacccaggtgtggctgagacactg gtagaggctgtgagcatgagtgcacttgagtgccagtaccagttccgttttgagcgctgg aactgcaccctggagggccgttaccgagccagcctgctcaagcgaggcttcaaggagacc gccttcctctatgccatctcctctgcgggcctgacacatgcactggccaaggcatgcagt gcaggccgcatggaacgctgcacgtgtgacgaggcacctgacctggagaaccgtgaagcc tggcagtggggtggctgtggagacaacctcaagtatagcagcaagtttgtcaaggagttc ctgggcaggcggtcgagcaaggatcttcgagcccgagtagacttccacaacaacctcgtg ggtgtgaaggtgatcaaggctggggtggagaccacctgcaaatgccatggcgtgtctggc tcctgcacagtgcggacctgctggcggcagctagcgcccttccacgaggtgggcaagcac ctgaaacacaagtatgagacggcacttaaggtgggcagcactaccaatgaagctaccggc gaggcaggcgccatctccccaccacggggccgggcctcagggtcaggaggtggtgatcca ctgccccgaacaccagagcttgtacacctggatgactctcccagcttctgcctggctggc cgcttctcccctggcactgcaggccgcaggtgccaccgtgagaaaaactgtgagagtatt tgctgtggccgtggccacaacacacagagccgggtggtaacaaggccctgccagtgccag gtacgctggtgctgctatgtggagtgcaggcaatgcacacagcgagaggaggtctacacc tgcaagggctga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103743015 Help Entry 103743015         CDS       T03372                                  Gene name Wnt11 Definition (RefSeq) Wnt family member 11   KO K01384   wingless-type MMTV integration site family, member 11 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103743015 (Wnt11)    04390 Hippo signaling pathway     103743015 (Wnt11)    04150 mTOR signaling pathway     103743015 (Wnt11)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103743015 (Wnt11)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103743015 (Wnt11)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103743015 (Wnt11)    05205 Proteoglycans in cancer     103743015 (Wnt11)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103743015 (Wnt11)    05226 Gastric cancer     103743015 (Wnt11)    05217 Basal cell carcinoma     103743015 (Wnt11)    05224 Breast cancer     103743015 (Wnt11)   09164 Neurodegenerative disease    05010 Alzheimer disease     103743015 (Wnt11)    05022 Pathways of neurodegeneration - multiple diseases     103743015 (Wnt11)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103743015 (Wnt11)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103743015 (Wnt11)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103743015 (Wnt11) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103743015 (Wnt11) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103743015 NCBI-ProteinID:  XP_008842451 LinkDB All DBs Position Un AA seq 354 aa AA seqDB search MKARPQVCEALLFALALHTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR SNLELMRTIVHAAREAMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK TGSQANKLMRLHNSEVGRQALRASLETKCKCHGVSGSCSIRTCWKGLQELWDVAADLKTR YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN KTSNGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK NT seq 1065 nt NT seq  +upstreamnt  +downstreamnt atgaaggcgcggccgcaggtctgcgaggcgctgctcttcgccctggctctccacactggc gtgtgctatggcatcaagtggctggctctatccaagacgccggcagccctggcgctcaac cagacgcagcactgcaaacagctagagggcttggtgtctgcgcaggtgcagctctgccgc agcaacctggagctcatgcgtaccatcgtgcacgctgctcgggaggccatgaaggcctgc cgcagggccttcgctgacatgcgctggaactgctcttccatcgagctcgcccccaactac ctgcttgacttggagagaggtacccgggaatcagccttcgtgtatgcgctgtcggccgct gccatcagccacgccatcgcccgggcctgcacctctggcgacctgcccggctgctcctgc ggccctgtcccaggtgagccacccgggcctgggaaccgctggggaggatgtgcggacaac ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct ctgcgtgcctccctggaaacgaagtgtaagtgccatggagtgtctggctcctgctccatc cgcacctgctggaaggggctacaggagctctgggatgtggctgccgacctcaagacccgc tacttgtcagccaccaaggtggtgcaccgacccatgggcacccgcaaacacttggttccc aaagacctggatatccggcctgtgaaggactcagaactggtctatctgcagagttcacct gacttctgtatgaagaatgagaaggtgggctcccacgggacccaagacaggcagtgcaac aagacctccaatggcagcgacagctgcgacctcatgtgctgtgggcgcggctacaacccc tacacagaccgcgtggtggagcggtgccactgcaagtaccactggtgttgctatgtcacc tgccgcaggtgtgagcgcacagtggaacgttatgtctgcaagtga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103743417 Help Entry 103743417         CDS       T03372                                  Gene name Wnt7b Definition (RefSeq) Wnt family member 7B   KO K00572   wingless-type MMTV integration site family, member 7 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103743417 (Wnt7b)    04390 Hippo signaling pathway     103743417 (Wnt7b)    04150 mTOR signaling pathway     103743417 (Wnt7b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103743417 (Wnt7b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103743417 (Wnt7b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103743417 (Wnt7b)    05205 Proteoglycans in cancer     103743417 (Wnt7b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103743417 (Wnt7b)    05226 Gastric cancer     103743417 (Wnt7b)    05217 Basal cell carcinoma     103743417 (Wnt7b)    05224 Breast cancer     103743417 (Wnt7b)   09164 Neurodegenerative disease    05010 Alzheimer disease     103743417 (Wnt7b)    05022 Pathways of neurodegeneration - multiple diseases     103743417 (Wnt7b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103743417 (Wnt7b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103743417 (Wnt7b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103743417 (Wnt7b) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103743417 (Wnt7b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103743417 NCBI-ProteinID:  XP_008842908 LinkDB All DBs Position Un AA seq 353 aa AA seqDB search MLLLSPRSALLSVYCPQIFLLLSSGSYLALSSVVALGANIICNKIPGLAPRQRAICQSRP DAIIVIGEGAQMGIDECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVA HAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNA RRLMNLHNNEAGRKVLEDRMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAV QVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNR TSQGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK NT seq 1062 nt NT seq  +upstreamnt  +downstreamnt atgctcctcctgtcgccgcggagcgcgcttctctccgtctattgcccgcagatctttctc ctcctgtccagcggcagctacctagcactgtcatccgtggtagccctgggagccaacatc atctgcaacaagattcctggcctggccccgcggcagcgtgccatctgccagagccgaccc gatgccatcatcgtgatcggggaaggggcgcagatgggcattgatgagtgccagtatcag ttccgctttggccgctggaactgctccgccctgggcgagaagaccgtcttcgggcaagag ctccgagtagggagccgtgaggccgctttcacatatgccatcaccgcagcaggcgtggca catgcagtcacggccgcctgcagccagggcaacctgagcaactgtggctgtgacagggag aagcaaggctactacaatcaggcggagggctggaagtggggcggctgctcagctgatgtg cgatacggcatcgacttctcccggcgcttcgtggatgcccgagagatcaagaagaacgcc aggcgcctcatgaatctccacaacaacgaggcgggcaggaaggttctggaggaccgcatg aagctggagtgtaagtgtcacggcgtgtcgggctcctgtaccaccaaaacctgctggacc acgctgcccaagttccgagaggtgggtcacctgctcaaggaaaagtacaacgccgccgtg caggtagaggtggtccgtgccagccgcctgcggcagcccaccttcctgcgcatcaaacag ctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaagtcacctaac tactgtgaggaggacgcggccacgggcagcgtgggcacacagggccgcctgtgcaaccgc acctcgcagggtgccgatggctgcgacaccatgtgctgcgggcgcggctacaacacgcac cagtacacaaaagtgtggcagtgtaactgcaaatttcactggtgctgcttcgtcaagtgc aacacgtgcagcgagcgcaccgaggtcttcacctgcaagtga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103743982 Help Entry 103743982         CDS       T03372                                  Gene name Wnt8b Definition (RefSeq) Wnt family member 8B   KO K00714   wingless-type MMTV integration site family, member 8 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103743982 (Wnt8b)    04390 Hippo signaling pathway     103743982 (Wnt8b)    04150 mTOR signaling pathway     103743982 (Wnt8b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103743982 (Wnt8b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103743982 (Wnt8b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103743982 (Wnt8b)    05205 Proteoglycans in cancer     103743982 (Wnt8b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103743982 (Wnt8b)    05226 Gastric cancer     103743982 (Wnt8b)    05217 Basal cell carcinoma     103743982 (Wnt8b)    05224 Breast cancer     103743982 (Wnt8b)   09164 Neurodegenerative disease    05010 Alzheimer disease     103743982 (Wnt8b)    05022 Pathways of neurodegeneration - multiple diseases     103743982 (Wnt8b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103743982 (Wnt8b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103743982 (Wnt8b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103743982 (Wnt8b) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103743982 (Wnt8b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103743982 NCBI-ProteinID:  XP_008843776 LinkDB All DBs Position Un AA seq 329 aa AA seqDB search MSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSHGGLRSAN RETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDNVGFGEAI SKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTCKCHGVSGSCTTQTCWLQLPEFR EVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRSISTRELVHLEDSPDYCLENKTL GLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEERRAETVSSCNCKFHWCCAVHCE QCRRRVTKYFCSRAERPPRGAAHKPGRKP NT seq 990 nt NT seq  +upstreamnt  +downstreamnt atgtcagtgaacaattttctgatgactggtccaaaggcttacctgatctactccagtagt gtggcagctggtgcgcagagtggaattgaagaatgtaaataccagtttgcctgggaccgc tggaactgccctgagagagccttacagctgtcgagccatggtggacttcgcagtgctaat cgggagacagcgtttgtacacgccatcagctctgctggggtcatgtacaccctgactaga aactgcagccttggagattttgacaactgtggctgtgatgactcccgcaatggacaactg gggggccaaggctggctgtggggaggctgcagtgataacgtgggtttcggagaggccatt tccaagcagtttgtggatgccctggagacaggacaggatgcccgggcagccatgaatctg cacaacaatgaggctggccgcaaggcggtgaagggaaccatgaaacgcacgtgcaagtgc cacggcgtgtccggcagctgcaccacgcagacctgctggctgcagctgccggagttccgc gaggtgggcgcgcacctgaaggagaagtatcacgcggcgctcaaggtggacctgctgcag ggtgcgggcaacagcgcggcgggtcgcggcgccatcgccgacaccttccgctccatctcc acgcgcgagctggtgcacctggaggactccccagactactgcctggagaacaagactcta gggctgctgggcaccgagggccgcgagtgcctgcgtcgcgggcgagcgctgggccgctgg gagcgtcgcagctgccgccggctgtgcggggactgcgggctggctgtggaggagcgccgc gccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgcggtccactgcgag cagtgccgccggcgggtcaccaagtacttctgcagccgcgcagagcggccgccgagaggc gccgcacacaaacctggaaggaaaccctaa

Nannospalax galili (Upper Galilee mountains blind mole rat): 103746395 Help Entry 103746395         CDS       T03372                                  Gene name Wnt4 Definition (RefSeq) Wnt family member 4   KO K00408   wingless-type MMTV integration site family, member 4 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04360   Axon guidance ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04919   Thyroid hormone signaling pathway ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103746395 (Wnt4)    04390 Hippo signaling pathway     103746395 (Wnt4)    04150 mTOR signaling pathway     103746395 (Wnt4)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103746395 (Wnt4)  09150 Organismal Systems   09152 Endocrine system    04919 Thyroid hormone signaling pathway     103746395 (Wnt4)    04916 Melanogenesis     103746395 (Wnt4)   09158 Development and regeneration    04360 Axon guidance     103746395 (Wnt4)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103746395 (Wnt4)    05205 Proteoglycans in cancer     103746395 (Wnt4)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103746395 (Wnt4)    05226 Gastric cancer     103746395 (Wnt4)    05217 Basal cell carcinoma     103746395 (Wnt4)    05224 Breast cancer     103746395 (Wnt4)   09164 Neurodegenerative disease    05010 Alzheimer disease     103746395 (Wnt4)    05022 Pathways of neurodegeneration - multiple diseases     103746395 (Wnt4)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103746395 (Wnt4)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103746395 (Wnt4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103746395 (Wnt4) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103746395 (Wnt4) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103746395 NCBI-ProteinID:  XP_008846777 LinkDB All DBs Position Un AA seq 296 aa AA seqDB search MCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAFVYAI SSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVDVRER SKGASSSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVGHALK EKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDIRSGVLGTRGRT CNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR NT seq 891 nt NT seq  +upstreamnt  +downstreamnt atgtgcaagcggaatctggaggtgatggactcggtgcgccgtggcgcccagttggccatt gaggagtgccagtaccagttccggaaccggcgctggaactgctccacacttgactccctg cccgtctttggcaaggtggtgactcaagggactcgggaggcggcgtttgtgtatgccatc tcttcagcaggtgtagcctttgcggtaacaagggcgtgcagcagtggagaactggaaaag tgtggctgtgaccggacggtgcatggggtcagcccacagggcttccaatggtcaggatgc tcggacaacatcgcctatggtgtggccttctcacagtcctttgtggacgtgcgggagaga agcaagggggcctcctctagccgggccctcatgaaccttcacaacaacgaggctggcagg aaggccatcctgacacacatgcgggtggaatgcaagtgccacggggtgtcaggttcctgt gaggtaaagacatgctggcgagcagtaccgcccttccgccaagtgggccatgcactgaag gagaagtttgatggggccaccgaagtggaacctcgccgtgtaggctcctccagggcactg gtgccacgtaacgcacagttcaagccacatacagatgaggacctggtgtacctggagccc agcccggacttctgtgagcaggacatacgcagtggtgtgctgggcacgagaggccgtaca tgcaacaagacgtctaaggccattgacggctgcgagctgctgtgctgcggccgtggcttc cacacggcacaggtagagctggctgaacgctgcagctgcaagttccattggtgctgcttc gtcaaatgccgccagtgccagcgacttgtggagctacacacgtgccggtga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103749032 Help Entry 103749032         CDS       T03372                                  Gene name Wnt5a Definition (RefSeq) Wnt family member 5A   KO K00444   wingless-type MMTV integration site family, member 5 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04360   Axon guidance ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103749032 (Wnt5a)    04390 Hippo signaling pathway     103749032 (Wnt5a)    04150 mTOR signaling pathway     103749032 (Wnt5a)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103749032 (Wnt5a)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103749032 (Wnt5a)   09158 Development and regeneration    04360 Axon guidance     103749032 (Wnt5a)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103749032 (Wnt5a)    05205 Proteoglycans in cancer     103749032 (Wnt5a)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103749032 (Wnt5a)    05226 Gastric cancer     103749032 (Wnt5a)    05217 Basal cell carcinoma     103749032 (Wnt5a)    05224 Breast cancer     103749032 (Wnt5a)   09164 Neurodegenerative disease    05010 Alzheimer disease     103749032 (Wnt5a)    05022 Pathways of neurodegeneration - multiple diseases     103749032 (Wnt5a)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103749032 (Wnt5a)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103749032 (Wnt5a)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103749032 (Wnt5a) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103749032 (Wnt5a) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103749032 NCBI-ProteinID:  XP_008850059 LinkDB All DBs Position Un AA seq 360 aa AA seqDB search MCSKFLLMALAIFFSFAQVEIEANSWWSLGVNNPVQMSEVYIIGAQPLCSQLAGLSQGQK KLCHLYQDHMQYIGEGAKTGIKECQYQFRHRRWNCSTVDNTSVFGRVMQIGSRETAFTYA VSAAGVVNAMSRACREGELSTCGCSRAARPKDLPRDWLWGGCGDNIDYGYRFAKEFVDAR ERERIHAKGSYESARILMNLHNNEAGRRTVYNLADVACKCHGVSGSCSLKTCWLQLADFR KVGDALKEKYDSAAAMRLNSRGKLVQVNSRFNSPTTQDLVYIDPSPDYCVRNESTGSLGT QGRLCNKTSEGMDGCELMCCGRGYDQFKTVQTERCHCKFHWCCYVKCKKCTEIVDQFVCK NT seq 1083 nt NT seq  +upstreamnt  +downstreamnt atgtgttccaagttcctcctaatggctctggccatatttttctccttcgcccaggttgaa atcgaagctaattcttggtggtccctaggtgtgaataaccctgttcagatgtcagaagta tatatcataggcgcacagcctctttgcagccaactggcaggactgtctcaaggacagaag aaactgtgccacttgtatcaggaccacatgcagtacattggagaaggtgcgaagacgggc atcaaagaatgccagtaccagttcaggcatcggagatggaactgcagcacggtggataac acctctgtctttggcagggtgatgcagataggcagcagagagacggccttcacttacgcc gtgagtgccgcgggagtggtgaatgccatgagccgagcttgccgagagggcgagctgtct acttgcggctgcagtcgggctgcgcgccccaaggacctgccgcgggactggctgtggggt ggctgcggcgacaacatagactatggctaccgcttcgccaaggagttcgtggacgcacgt gagcgggagcgcatccacgccaagggctcctatgagagcgcacgcatcctcatgaacctg cataacaacgaggcaggccgaaggacggtgtacaacctggcagacgtagcctgcaagtgc catggggtgtccggctcatgtagcctcaagacgtgctggctgcagctagcggacttccgc aaggtgggggatgccctcaaggagaagtatgacagcgcagcagccatgcggctcaacagc aggggcaagctggtgcaggtcaacagccgcttcaactcgcccaccacgcaggacctggtc tatatcgacccgagtccggactactgcgtgcgcaatgagagcacgggctcgctgggcaca cagggccgcctgtgcaacaagacatcggagggcatggatggctgcgaactcatgtgctgt ggccgaggctatgaccagttcaagacagtgcagaccgagcgctgccactgcaagttccac tggtgctgctatgtcaagtgcaagaagtgcacggagatcgtggaccagttcgtgtgcaaa tag

Nannospalax galili (Upper Galilee mountains blind mole rat): 103750565 Help Entry 103750565         CDS       T03372                                  Gene name Wnt10b Definition (RefSeq) Wnt family member 10B   KO K01357   wingless-type MMTV integration site family, member 10 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103750565 (Wnt10b)    04390 Hippo signaling pathway     103750565 (Wnt10b)    04150 mTOR signaling pathway     103750565 (Wnt10b)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103750565 (Wnt10b)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103750565 (Wnt10b)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103750565 (Wnt10b)    05205 Proteoglycans in cancer     103750565 (Wnt10b)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103750565 (Wnt10b)    05226 Gastric cancer     103750565 (Wnt10b)    05217 Basal cell carcinoma     103750565 (Wnt10b)    05224 Breast cancer     103750565 (Wnt10b)   09164 Neurodegenerative disease    05010 Alzheimer disease     103750565 (Wnt10b)    05022 Pathways of neurodegeneration - multiple diseases     103750565 (Wnt10b)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103750565 (Wnt10b)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103750565 (Wnt10b)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103750565 (Wnt10b) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103750565 (Wnt10b) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF5586 Motif Other DBs NCBI-GeneID:  103750565 NCBI-ProteinID:  XP_008851892 LinkDB All DBs Position Un AA seq 389 aa AA seqDB search MLEEPRSRPPPSGLAGLLFLALCSRALSNEILGLKVPGEPPLTANTVCLTLSGLSKRQLG LCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLEALSRGKSFPHSVPSP VPGSGPNPGPQDTWEWAGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLSRAIFIDTHNRNSGAFQPRLR PRRLSGELVYFEKSPDFCERDPTVGSPGTRGRVCNKTSRLLDGCGSLCCGRGHNVLRQTR VERCHCRFHWCCYVLCDECKVTEWVNVCK NT seq 1170 nt NT seq  +upstreamnt  +downstreamnt atgctggaggagccccggtctcgacctccgccctcgggcctcgcgggtctcctgttcttg gccttgtgcagtcgggctctaagcaatgagattctgggcctgaaagttcctggtgagccg ccgctgactgccaacaccgtgtgcttgaccctgtcgggtttgagtaagcgacagctaggc ctgtgtctacgcagccccgacgtgacggcgtcggcgcttcagggtctgcacatcgcggtt cacgagtgtcagcaccagcttcgggaccagcgctggaactgctctgccctggagggcggt ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgtgagagtgctttctcc ttctccatgctggctgctggggtcatgcatgctgttgccacagcctgcagcctgggcaag ctggtgagctgtggctgcggctggaagggcagtggtgagcaggaccggcttcgagccaaa ctgctgcagctggaggcactgtcccggggcaagagttttccccactcagtgcccagccct gtccctggttctggccccaatcctggcccccaggacacatgggaatgggctggctgtaac catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc agggacatccaggcacgaatgcgaatccacaacaacagggtggggcgccaggtggtaacc gaaaacctgaagcggaagtgcaagtgtcatggcacatcaggcagctgccagttcaagaca tgctggagggcagcccctgagttccgagctgtaggggcagcactgagagagcggttgagc agagccatcttcatcgatacccataaccgcaattctggagctttccagccccgcctgcga ccccgtcgcctctcaggagagctggtctactttgagaagtccccagacttctgtgagagg gaccccacggtgggctccccaggcacaagaggccgggtctgcaacaagaccagccgcctg ttggatggctgtggcagcctgtgctgtggccgagggcacaacgtgctccgacagacacga gttgagcgctgccattgccgtttccactggtgctgctatgtgctgtgtgatgagtgcaaa gtcacagaatgggtcaatgtgtgtaagtga

Nannospalax galili (Upper Galilee mountains blind mole rat): 103750567 Help Entry 103750567         CDS       T03372                                  Gene name Wnt1 Definition (RefSeq) Wnt family member 1   KO K03209   wingless-type MMTV integration site family, member 1 Organism ngi  Nannospalax galili (Upper Galilee mountains blind mole rat) Pathway ngi04150   mTOR signaling pathway ngi04310   Wnt signaling pathway ngi04390   Hippo signaling pathway ngi04550   Signaling pathways regulating pluripotency of stem cells ngi04916   Melanogenesis ngi04934   Cushing syndrome ngi05010   Alzheimer disease ngi05022   Pathways of neurodegeneration - multiple diseases ngi05165   Human papillomavirus infection ngi05200   Pathways in cancer ngi05205   Proteoglycans in cancer ngi05217   Basal cell carcinoma ngi05224   Breast cancer ngi05225   Hepatocellular carcinoma ngi05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ngi00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     103750567 (Wnt1)    04390 Hippo signaling pathway     103750567 (Wnt1)    04150 mTOR signaling pathway     103750567 (Wnt1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     103750567 (Wnt1)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     103750567 (Wnt1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     103750567 (Wnt1)    05205 Proteoglycans in cancer     103750567 (Wnt1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     103750567 (Wnt1)    05226 Gastric cancer     103750567 (Wnt1)    05217 Basal cell carcinoma     103750567 (Wnt1)    05224 Breast cancer     103750567 (Wnt1)   09164 Neurodegenerative disease    05010 Alzheimer disease     103750567 (Wnt1)    05022 Pathways of neurodegeneration - multiple diseases     103750567 (Wnt1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     103750567 (Wnt1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     103750567 (Wnt1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ngi00536]     103750567 (Wnt1) Glycosaminoglycan binding proteins [BR:ngi00536]  Heparan sulfate / Heparin   Morphogens    103750567 (Wnt1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  103750567 NCBI-ProteinID:  XP_008851894 LinkDB All DBs Position Un AA seq 370 aa AA seqDB search MGFWTLLPSWVSAMLLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTAPGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRVLHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggttctggacgctgctgcccagctgggtttctgctatgttgctactggcactggcc gctctgcccgcagccctggccgccaacagcagtggccgatggtggggcatcgtaaatgta gcctcctccacgaatctgctgacggactccaagagtctgcaactggtgctagagcccagt ctgcagttgctgagccgcaaacagcggcggctgatccgccagaacccggggatcctgcac agcgtgagcggagggctgcagagcgcagtgcgcgagtgcaagtggcagttccggaaccgc cgctggaactgccctactgctcccgggccccacctcttcggcaaaatcgtcaaccgaggc tgccgggaaacagcgtttattttcgccatcacctccgccggggtcacacattcggtggcg cgctcctgctccgagggctccatcgagtcttgcacttgtgactaccgccggcgcggcccc ggggggcccgactggcactggggaggttgcagcgacaacatcgatttcggccgcctcttt ggccgagagttcgtggactctggggagaaggggcgggacctgcgctttctcatgaacctg cacaacaacgaggctggccgcacgaccgtgttctctgagatgcgccaggagtgcaagtgc catgggatgtctggctcgtgcaccgtgcgcacgtgctggatgcggctgcccacgctgcgt gctgtcggtgacgtgctgcgcgaccgcttcgacggcgcctctcgagtcctctatggcaac cgcggtagcaaccgcgcttcccgggccgagctgctgcgcctggagcccgaagaccctgcg cacaagccgccctcccctcacgacctcgtctacttcgagaaatcgcccaacttctgcacg tacagcggacgcttgggtacggcgggcacggcagggcgtgcttgcaacagctcttctcct gcgctggacggctgcgagttgctctgctgtggccggggccaccgcacgcgcacgcagcgc gtcactgagcgttgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc acgcacacgcgcgtactgcatgagtgtttgtga

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