Vulpes vulpes (red fox): 112907938 Help Entry 112907938         CDS       T05911                                  Gene name WNT2B Definition (RefSeq) protein Wnt-2b isoform X1   KO K00182   wingless-type MMTV integration site family, member 2 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112907938 (WNT2B)    04390 Hippo signaling pathway     112907938 (WNT2B)    04150 mTOR signaling pathway     112907938 (WNT2B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112907938 (WNT2B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112907938 (WNT2B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112907938 (WNT2B)    05205 Proteoglycans in cancer     112907938 (WNT2B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112907938 (WNT2B)    05226 Gastric cancer     112907938 (WNT2B)    05217 Basal cell carcinoma     112907938 (WNT2B)    05224 Breast cancer     112907938 (WNT2B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112907938 (WNT2B)    05022 Pathways of neurodegeneration - multiple diseases     112907938 (WNT2B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112907938 (WNT2B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112907938 (WNT2B) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112907938 (WNT2B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112907938 NCBI-ProteinID:  XP_025839071 UniProt:  A0A3Q7RAF8 LinkDB All DBs Position Unknown AA seq 393 aa AA seqDB search MLEPGGAEDAAQLPPRRARAPVPTLAPGPVAPDGARASSRLGLACLLLLLLLTLPARVDT SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT NT seq 1182 nt NT seq  +upstreamnt  +downstreamnt atgctggagccgggcggtgcggaggacgccgcgcagctgccccccaggcgcgcccgcgcc cctgtgcccacgctcgcgccaggccccgtggcccccgacggcgcccgggcttcttcccgc ctcggtcttgcctgcctgctgctgctgctgctgctgacgctgccggcccgtgtagacacg tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaacatccctggtctg gtgagtcggcagcggcagctgtgccagcgttacccagatatcatgcgctcagtgggcgag ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc accacgctggaccgggaccacactgtctttggccgagtcatgctcagaagtagccgggaa gcagcatttgtatatgccatctcatcagcaggggtggtccatgctatcacccgtgcctgt agccagggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgac caacgtggggattttgactggggtggctgcagtgacaacatccactatggtgttcgtttt gccaaggcctttgtggacgccaaggaaaagaggcttaaggatgcccgggccctcatgaac ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgtaag tgccatggcgtaagtggctcctgtactctacgcacctgctggcgtgcgctctcagacttc cgccgcacaggtgactacctgcggcggcgctatgatggtgctgtgcaggtgacagcaacc caggatggtgccaacttcacagcagcccgccaaggctaccgccgtgccacccggactgac cttgtctactttgacaactccccagattactgtgtcttggacaaggctgcaggttcccta ggcactgcgggccgagtctgcagcaagacatctaaagggacagatggttgtgaaatcatg tgctgtggccgaggatatgacacaactcgagtcacccgtgtcacccagtgtgaatgcaaa ttccactggtgctgtgcagtgcggtgcaaggagtgcagaaacactgtggacgtccatact tgcaaggcccccaagaaggcagagtggctggaccagacctga

Vulpes vulpes (red fox): 112909974 Help Entry 112909974         CDS       T05911                                  Gene name WNT5A Definition (RefSeq) protein Wnt-5a isoform X1   KO K00444   wingless-type MMTV integration site family, member 5 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04360   Axon guidance vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112909974 (WNT5A)    04390 Hippo signaling pathway     112909974 (WNT5A)    04150 mTOR signaling pathway     112909974 (WNT5A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112909974 (WNT5A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112909974 (WNT5A)   09158 Development and regeneration    04360 Axon guidance     112909974 (WNT5A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112909974 (WNT5A)    05205 Proteoglycans in cancer     112909974 (WNT5A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112909974 (WNT5A)    05226 Gastric cancer     112909974 (WNT5A)    05217 Basal cell carcinoma     112909974 (WNT5A)    05224 Breast cancer     112909974 (WNT5A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112909974 (WNT5A)    05022 Pathways of neurodegeneration - multiple diseases     112909974 (WNT5A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112909974 (WNT5A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112909974 (WNT5A) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112909974 (WNT5A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112909974 NCBI-ProteinID:  XP_025841969 UniProt:  A0A3Q7R770 LinkDB All DBs Position Unknown AA seq 380 aa AA seqDB search MKKSIGILRPGVALGTAGSAMSSKFFLMALAIFFSFAQVVIEANSWWSLGMNNPVQMSEV YIIGAQPLCSQLAGLSQGQKKLCHLYQDHMQYIGEGAKTGIKECQYQFRHRRWNCSTVDN TSVFGRVMQIGSRETAFTYAVSAAGVVNAMSRACREGELSTCGCSRAARPKDLPRDWLWG GCGDNIDYGYRFAKEFVDARERERIHAKGSYESARILMNLHNNEAGRRTVYNLADVACKC HGVSGSCSLKTCWLQLADFRKVGDALKEKYDSAAAMRLNSRGKLVQVNSRFNSPTTQDLV YIDPSPDYCVRNESTGSLGTQGRLCNKTSEGMDGCELMCCGRGYDQFKTVQTERCHCKFH WCCYVKCKKCTEIVDQFVCK NT seq 1143 nt NT seq  +upstreamnt  +downstreamnt atgaagaagtcgattggaatattaaggccaggagttgctttggggacggctggaagtgca atgtcttccaagttcttcctaatggctttggccatatttttctccttcgcccaggttgta atagaagccaattcttggtggtcgctaggtatgaataaccctgttcagatgtcagaagta tatatcataggagcgcagcctctctgcagccagctggcaggactttctcaaggacagaag aaactgtgccacttgtatcaggaccacatgcagtacattggagaaggcgcaaagacgggc atcaaagagtgccagtatcaattccggcatcggaggtggaactgcagcaccgtggataac acctccgtttttggcagggtcatgcagataggcagccgcgagacggccttcacgtacgcg gtgagcgccgcgggggtggtgaacgccatgagccgcgcgtgccgcgagggcgagctgtcc acctgcggctgcagccgggccgcgcgccccaaggacctgccgcgggactggctgtggggc ggctgcggggacaacatcgactacggctaccgcttcgccaaggagttcgtggacgcgcgc gagcgggagcgcatccacgccaagggctcctacgagagcgcgcgcatcctcatgaacctg cacaacaacgaggccggccgcaggacggtgtacaacctggccgacgtggcctgcaagtgc cacggggtgtcgggctcgtgtagcctcaagacgtgctggctgcagctggccgacttccgc aaggtgggcgacgccctgaaggagaagtacgacagcgcagcggccatgcggctcaacagc cggggcaagctggtgcaggtcaacagccgcttcaactcgcccaccacgcaggacctggtc tacatcgaccccagccccgactactgcgtgcgcaacgagagcaccggctcgctgggcacg cagggccgcctgtgcaacaagacgtccgagggcatggacggctgcgagctcatgtgctgc ggccgcggctacgaccagttcaagaccgtgcagacggagcgctgccactgcaagttccac tggtgctgctacgtcaagtgcaagaagtgcacggagatcgtggaccagttcgtgtgcaaa tag

Vulpes vulpes (red fox): 112910612 Help Entry 112910612         CDS       T05911                                  Gene name WNT16 Definition (RefSeq) protein Wnt-16   KO K01558   wingless-type MMTV integration site family, member 16 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05202   Transcriptional misregulation in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112910612 (WNT16)    04390 Hippo signaling pathway     112910612 (WNT16)    04150 mTOR signaling pathway     112910612 (WNT16)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112910612 (WNT16)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112910612 (WNT16)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112910612 (WNT16)    05202 Transcriptional misregulation in cancer     112910612 (WNT16)    05205 Proteoglycans in cancer     112910612 (WNT16)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112910612 (WNT16)    05226 Gastric cancer     112910612 (WNT16)    05217 Basal cell carcinoma     112910612 (WNT16)    05224 Breast cancer     112910612 (WNT16)   09164 Neurodegenerative disease    05010 Alzheimer disease     112910612 (WNT16)    05022 Pathways of neurodegeneration - multiple diseases     112910612 (WNT16)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112910612 (WNT16)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112910612 (WNT16) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112910612 (WNT16) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112910612 NCBI-ProteinID:  XP_025842602 UniProt:  A0A3Q7RAQ0 LinkDB All DBs Position Unknown AA seq 302 aa AA seqDB search MRGRQPWKGPSAQPGACDPLAPHIPRDQKEDLLWTKPDRDTALSFSNLCFVLGTKETAFI YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE KVGRLLKDKYENSIQISDKIQRKVRRRDKDQRRVPIRKDDLLYVNKSPNYCVEDKKLGIP GTRGRECNRTSEGAGGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT CK NT seq 909 nt NT seq  +upstreamnt  +downstreamnt atgcgaggccgccagccctggaaaggtccatcggcccagcccggagcctgcgaccccctc gctcctcacatcccaagggaccaaaaggaagatttgttatggacaaaaccagacagagat acggctctttcattcagcaatttatgttttgttctaggcaccaaggaaacagcatttatt tatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagtgccggcaac atgacggagtgctcctgtgacaccaccctacagaacggtggctcagcgagcgaaggctgg cactgggggggctgctctgatgatgtccagtatggcatgtggttcagcagaaagttccta gatttccccatcagaaacaccacaggaaaagaaagcaaagtactgttagcaatgaacctg cacaacaacgaagctggaaggcaggctgtcgccaagctcatgtcggtggactgccgctgt cacggggtctcgggctcctgcgccgtgaagacctgctggaaaaccatgtcctcgttcgag aaggtcggccggctgctgaaggacaagtacgaaaacagtatccagatctcagacaaaata cagcggaaggtgcgcaggagagacaaagaccagaggcgggtccccattcgcaaggacgac ctgctgtacgtcaacaagtcccccaactactgcgtggaggacaagaagctgggcatcccg ggcacgcggggccgcgagtgcaaccgcacctccgagggcgccggcggctgcaacctgctg tgctgcggccgcggctacaacacgcacgtggtcaggcacgtggagaggtgcgagtgcaag ttcatctggtgctgctacgttcgctgccggcgctgtgagagcatgaccgacgtgcacacc tgcaagtag

Vulpes vulpes (red fox): 112911970 Help Entry 112911970         CDS       T05911                                  Gene name WNT3A Definition (RefSeq) protein Wnt-3a   KO K00312   wingless-type MMTV integration site family, member 3 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05206   MicroRNAs in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112911970 (WNT3A)    04390 Hippo signaling pathway     112911970 (WNT3A)    04150 mTOR signaling pathway     112911970 (WNT3A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112911970 (WNT3A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112911970 (WNT3A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112911970 (WNT3A)    05206 MicroRNAs in cancer     112911970 (WNT3A)    05205 Proteoglycans in cancer     112911970 (WNT3A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112911970 (WNT3A)    05226 Gastric cancer     112911970 (WNT3A)    05217 Basal cell carcinoma     112911970 (WNT3A)    05224 Breast cancer     112911970 (WNT3A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112911970 (WNT3A)    05022 Pathways of neurodegeneration - multiple diseases     112911970 (WNT3A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112911970 (WNT3A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112911970 (WNT3A) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112911970 (WNT3A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112911970 NCBI-ProteinID:  XP_025844475 UniProt:  A0A3Q7SQN2 LinkDB All DBs Position Unknown AA seq 352 aa AA seqDB search MALLGYFLFLYGLKQALGSYPIWWSLAVGPQYSSLGTQPILCASIPGLVPKQLRFCRNYV EIMPSVADGMKISIQECQHQFRGRRWNCTTVNNSLAIFGPVLDKATRESAFVHAIASAGV AFAVTRSCAEGSAAICGCSSRHQGSPGEGWKWGGCSEDIEFGGMVSREFADARENRPDAR SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRSIGDFLKDKYDSASE MVVEKHRESRGWVETLRPRYSYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVS SHGIDGCDLLCCGRGHNARTEQRREKCHCVFHWCCYVSCQECARVYDVHTCK NT seq 1059 nt NT seq  +upstreamnt  +downstreamnt atggccctgctcgggtacttcttattcctctacggcctgaagcaggcgctgggcagctac ccgatctggtggtccctggccgtcgggccccagtactcatccctgggcactcagcccatc ctgtgcgccagcatcccaggcctggtacccaagcagctgcgcttctgccggaactacgtg gagatcatgcccagcgtggcggacggcatgaagatcagcatccaggagtgccagcaccag ttccgcgggcgccgctggaactgcaccacagtcaacaacagcctggccatcttcggccct gtgctggacaaagccacccgggagtctgcctttgtgcacgccatcgcctcggccggcgtg gccttcgctgtgacacgctcatgtgcggagggctccgctgccatctgtggctgcagcagc cgccaccagggctcaccaggtgagggctggaagtggggaggctgcagcgaggacatcgag tttggtggcatggtgtcccgggaattcgctgacgcacgggagaaccggccagacgcccgc tccgccatgaaccgccacaacaatgaggccggacgccaggccatcgccagccacatgcat ctcaagtgcaagtgccacgggctgtcgggcagttgcgaggtgaagacctgctggtggtca cagcccgacttccgctccatcggagacttcctcaaggacaagtacgacagcgcctccgag atggtggtggagaagcaccgcgagtcgcgcggctgggtggagacgctgcggccccgctac agctacttcaaggtgcccacggagcgcgaccttgtgtactacgaggcctcgcccaacttc tgcgagcccaaccccgagaccggctcgttcggcacccgcgaccgcacgtgcaacgtgagc tcgcatggcatcgacggctgcgacctgctgtgctgtggccgcggccacaacgcgcgcacc gagcagcgccgagagaagtgccactgcgtcttccactggtgctgctacgtgagctgccag gagtgcgcgcgcgtctacgacgtgcacacctgcaagtag

Vulpes vulpes (red fox): 112911976 Help Entry 112911976         CDS       T05911                                  Gene name WNT9A Definition (RefSeq) protein Wnt-9a   KO K01064   wingless-type MMTV integration site family, member 9 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112911976 (WNT9A)    04390 Hippo signaling pathway     112911976 (WNT9A)    04150 mTOR signaling pathway     112911976 (WNT9A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112911976 (WNT9A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112911976 (WNT9A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112911976 (WNT9A)    05205 Proteoglycans in cancer     112911976 (WNT9A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112911976 (WNT9A)    05226 Gastric cancer     112911976 (WNT9A)    05217 Basal cell carcinoma     112911976 (WNT9A)    05224 Breast cancer     112911976 (WNT9A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112911976 (WNT9A)    05022 Pathways of neurodegeneration - multiple diseases     112911976 (WNT9A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112911976 (WNT9A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112911976 (WNT9A) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112911976 (WNT9A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Clr5 Motif Other DBs NCBI-GeneID:  112911976 NCBI-ProteinID:  XP_025844488 UniProt:  A0A3Q7RGT8 LinkDB All DBs Position Unknown AA seq 388 aa AA seqDB search MAVWPQVHGESRQPGSQLCLPALPPAQPRVCLLGFRHTLRLSAACLLPALLLCGGLTGSE PLTILPLTLEPEAAAQAHYKACDRLKLERKQRRMCRRDPGVAETLVEAVSMSALECQYQF RFERWNCTLEGRYRASLLKRGFKETAFLYAISSAGLTHALAKACSAGRMERCTCDEAPDL ENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKDLRARVDFHNNLVGVKVIKAGVETTCKC HGVSGSCTVRTCWRQLAPFHEVGKRLKHKYETALKVGSTTNEATGEAGAISPPRGRATGT SGSDPLPRTPELVHLDDSPSFCLASRFSPGTAGRRCHREKNCESICCGRGHNTQSRVVTR PCQCQVRWCCYVECRQCTQREEVYTCKS NT seq 1167 nt NT seq  +upstreamnt  +downstreamnt atggccgtctggccgcaggtccacggtgagtcacggcagcccggcagccagctgtgcctt cccgctctgccgccggcccagcctcgggtctgcttactaggcttcagacacaccctacgc ttgtctgcagcatgtctgctgccagccctgctgctgtgtggagggctgactggcagcgag cccctgaccatcctcccgctgaccctggagcccgaggctgcagcgcaggcacactacaag gcctgcgaccgactgaagctggagcgcaagcagaggcgcatgtgccgccgagacccaggt gtggccgagacgctggtggaggcggtcagcatgagcgccctggagtgccagtaccagttc cggttcgagcgctggaactgtactctggagggtcgctaccgggccagcctgctcaagcga ggcttcaaggagactgccttcctctacgccatctcatctgcgggcctgacccatgcgctg gccaaggcgtgcagcgcgggccgcatggagcgctgcacctgcgacgaggccccagacctg gagaaccgggaggcctggcagtggggtggctgcggggacaacctcaagtacagcagcaag ttcgtcaaggagttcctgggccggaggtcgagcaaggacctgcgagcacgcgtggacttc cacaacaacctcgtgggtgtgaaggtaatcaaagccggggtggagaccacgtgtaagtgc catggtgtgtcaggctcctgcaccgtgcggacatgctggcggcagctggcacccttccat gaggtgggcaagcgcctgaaacacaagtatgagacggcgctcaaggtgggcagcaccacc aacgaggccactggtgaggccggtgccatctcgccacctcggggccgggctacagggaca agcggcagtgacccgttgccccgcacaccagagctcgtgcacctggatgactcgccgagc ttctgcttggccagccgcttttccccaggcactgctggccgcaggtgccaccgggagaag aactgtgagagcatctgctgtgggcgtggccacaacacgcagagccgggtggtgacacgg ccgtgccagtgccaggtgcgctggtgctgctatgtggagtgcaggcagtgtacccagcgt gaggaggtctacacctgcaagagctga

Vulpes vulpes (red fox): 112914456 Help Entry 112914456         CDS       T05911                                  Gene name WNT7A Definition (RefSeq) protein Wnt-7a   KO K00572   wingless-type MMTV integration site family, member 7 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112914456 (WNT7A)    04390 Hippo signaling pathway     112914456 (WNT7A)    04150 mTOR signaling pathway     112914456 (WNT7A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112914456 (WNT7A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112914456 (WNT7A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112914456 (WNT7A)    05205 Proteoglycans in cancer     112914456 (WNT7A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112914456 (WNT7A)    05226 Gastric cancer     112914456 (WNT7A)    05217 Basal cell carcinoma     112914456 (WNT7A)    05224 Breast cancer     112914456 (WNT7A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112914456 (WNT7A)    05022 Pathways of neurodegeneration - multiple diseases     112914456 (WNT7A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112914456 (WNT7A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112914456 (WNT7A) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112914456 (WNT7A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt COG6 Motif Other DBs NCBI-GeneID:  112914456 NCBI-ProteinID:  XP_025847338 UniProt:  A0A3Q7RQ31 LinkDB All DBs Position Unknown AA seq 349 aa AA seqDB search MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEVYTCK NT seq 1050 nt NT seq  +upstreamnt  +downstreamnt atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac ctccggatcggtggcttctcctccgtggtagctctgggcgcgagcatcatctgtaacaag atcccgggcctggctcccagacagcgggcgatatgccagagccgccccgacgccatcatc gtcataggagaaggctcgcaaatgggcctcgacgagtgtcagtttcagttccgcaatggc cgctggaactgctcagccctgggggagcgcaccgtcttcgggaaggagctcaaagtgggg agccgggaggctgccttcacctacgccatcatcgctgccggcgtggcccacgccatcacg gccgcctgcacccaaggcaacctgagtgactgtggctgcgacaaggagaagcaaggccag taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg aacttgcacaataacgaggcgggccgaaagatcctggaggaaaacatgaagctggagtgc aagtgccacggtgtgtccggctcgtgcaccaccaagacgtgctggaccacactgccacag ttccgcgagctgggctacgtgctcaaggacaagtacaacgaggccgtccacgtggagccg gtgcgcgccagccgcaacaagcggcccaccttcctgaagatcaagaagccgctgtcctac cgcaagcccatggacacagacctggtgtacatcgagaagtcgcccaactactgcgaggag gacccggtgacgggcagcgtgggcacgcagggccgcgcctgcaacaagacggccccgcag gccagcggctgtgacctcatgtgctgcggtcgcggctacaacacccaccagtacgcccgc gtgtggcagtgcaactgcaagtttcactggtgctgttatgtcaagtgcaacacctgcagc gagcgtaccgaggtgtacacgtgcaagtga

Vulpes vulpes (red fox): 112914893 Help Entry 112914893         CDS       T05911                                  Gene name WNT8B Definition (RefSeq) protein Wnt-8b   KO K00714   wingless-type MMTV integration site family, member 8 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112914893 (WNT8B)    04390 Hippo signaling pathway     112914893 (WNT8B)    04150 mTOR signaling pathway     112914893 (WNT8B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112914893 (WNT8B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112914893 (WNT8B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112914893 (WNT8B)    05205 Proteoglycans in cancer     112914893 (WNT8B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112914893 (WNT8B)    05226 Gastric cancer     112914893 (WNT8B)    05217 Basal cell carcinoma     112914893 (WNT8B)    05224 Breast cancer     112914893 (WNT8B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112914893 (WNT8B)    05022 Pathways of neurodegeneration - multiple diseases     112914893 (WNT8B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112914893 (WNT8B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112914893 (WNT8B) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112914893 (WNT8B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112914893 NCBI-ProteinID:  XP_025847988 UniProt:  A0A3Q7RS55 LinkDB All DBs Position Unknown AA seq 351 aa AA seqDB search MLLTKPSVCIFLFTCILRLGYTWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAW DRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNG QLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTC KCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRS ISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEE RRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKS NT seq 1056 nt NT seq  +upstreamnt  +downstreamnt atgttgcttacgaagccttctgtgtgcatcttccttttcacctgtatcctccgacttggc tacacctggtcagtgaacaatttcctgatgactggtccaaaggcttacctgatctattcc agcagtgtggcagctggtgcccagagtggtattgaagaatgcaaatatcagtttgcctgg gaccgatggaactgccctgagagagccctgcagctgtccagccatggcggccttcgcagt gctaatcgggagacagcgtttgtacacgccatcagttctgctggggtcatgtacactctg actaggaactgcagccttggagactttgacaactgtggctgtgacgactcccgcaacggg cagctgggtggccaaggctggctgtggggaggctgtagtgacaacgtgggcttcggagaa gcaatatccaagcagttcgtcgatgccctagagacaggacaggatgcccgggcagccatg aacctgcacaacaatgaggctggccgcaaggcggtgaagggcaccatgaaacgcacgtgt aagtgccacggtgtgtctggcagctgcaccacgcagacctgctggctgcagctgcctgag ttccgcgaggtgggcgcacacctgaaggagaagtaccacgcagctctcaaggtggacctg ctgcagggcgctggcaacagtgctgccggccggggtgccatcgccgacaccttccgctcc atctccacgcgggagctggtgcacttggaggactccccggactactgcctggagaacaaa acgctaggactgctgggtactgaaggccgagagtgcctgcggcgtgggcgggccctgggc cgctgggagcgccgcagctgccgccggctctgcggggactgcgggctggcggtggaggag cgccgggccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgccgtccgc tgcgagcagtgccgccggcgggttaccaagtacttctgcagccgcgctgagcggccgcgg gggggcgcagcgcacaagcccgggagaaaatcctga

Vulpes vulpes (red fox): 112917420 Help Entry 112917420         CDS       T05911                                  Gene name WNT5B Definition (RefSeq) protein Wnt-5b   KO K00444   wingless-type MMTV integration site family, member 5 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04360   Axon guidance vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112917420 (WNT5B)    04390 Hippo signaling pathway     112917420 (WNT5B)    04150 mTOR signaling pathway     112917420 (WNT5B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112917420 (WNT5B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112917420 (WNT5B)   09158 Development and regeneration    04360 Axon guidance     112917420 (WNT5B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112917420 (WNT5B)    05205 Proteoglycans in cancer     112917420 (WNT5B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112917420 (WNT5B)    05226 Gastric cancer     112917420 (WNT5B)    05217 Basal cell carcinoma     112917420 (WNT5B)    05224 Breast cancer     112917420 (WNT5B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112917420 (WNT5B)    05022 Pathways of neurodegeneration - multiple diseases     112917420 (WNT5B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112917420 (WNT5B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112917420 (WNT5B) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112917420 (WNT5B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112917420 NCBI-ProteinID:  XP_025851259 UniProt:  A0A3Q7RZZ2 LinkDB All DBs Position Unknown AA seq 358 aa AA seqDB search MPSRLLLTAALLSSWAHLPAEASSWWSLAMSPVQRPEMFIIGAQPVCSQLPGLSPGQRKL CQLYQEHMAYIGEGAKTGIKECQYQFRQRRWNCSTVDNMSVFGRVMQIGSRETAFAYAVS AAGVADAVSRACREGELSTCGCSRAARPQDLPRDWLWGGCGDNVDYGYRFAKEFVDARER EKNFAKGSEEQARVLMNLQNNEAXRRAVYKMADVACKCHGVSGSCSLKTCWLQLAEFRKV GDQLKEKYDSAAAMRITRKGKLELVNSRFNQPTPEDLVYVDSSPDYCLRNETTGSLGTQG RLCNKTSEGMDGCELMCCGRGYDQFKSVQVERCHCKFHWCCYVKCKKCTEIVDQYVCK NT seq 1077 nt NT seq  +upstreamnt  +downstreamnt atgcccagccggctgctgctcaccgctgcactgctgtccagctgggctcatcttccggcc gaagccagctcctggtggtcattagctatgagccctgtacagagacctgagatgtttatc atcggtgcccagcccgtgtgcagccagcttcctgggctctcccctggccagaggaagctg tgccagttgtaccaggagcacatggcctacatcggggagggagccaagacgggcatcaag gagtgccagtaccagttccgtcagaggcggtggaactgcagcactgtggacaacatgtct gtctttgggagagtcatgcagatagggagccgggagaccgccttcgcctacgcggtgagc gccgcgggcgtggcggacgccgtgagccgggcctgccgcgagggcgagctgtccacctgc ggctgcagccgggccgcgcggccccaggacctgccccgggactggctgtggggcggctgc ggggacaacgtggactacggctaccgctttgctaaagagttcgtggacgcccgcgagcgg gagaagaacttcgccaaggggtcggaggagcaggcccgagtgctcatgaacctgcagaac aacgaggcggngcggagggctgtgtataagatggcagatgtagcctgcaagtgccacggc gtctcagggtcctgcagcctcaagacctgctggctccagctggccgagttccgcaaagta ggggaccagctgaaggagaagtatgacagcgcagccgccatgcgcatcacccgcaagggc aaactggagctggtcaacagccgcttcaaccagcccacccctgaggacctggtctatgtg gactccagcccagactactgtctgcgcaatgagaccacgggctccctgggtacccagggc cgcctctgcaacaagacctcggagggcatggatggctgcgagctcatgtgctgtggccgt ggctatgaccagttcaagagcgtccaggtggagcgctgccactgcaagttccactggtgc tgctatgtcaagtgcaagaagtgcaccgagatcgtcgaccagtatgtctgtaaatag

Vulpes vulpes (red fox): 112920632 Help Entry 112920632         CDS       T05911                                  Gene name WNT9B Definition (RefSeq) protein Wnt-9b   KO K01064   wingless-type MMTV integration site family, member 9 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112920632 (WNT9B)    04390 Hippo signaling pathway     112920632 (WNT9B)    04150 mTOR signaling pathway     112920632 (WNT9B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112920632 (WNT9B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112920632 (WNT9B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112920632 (WNT9B)    05205 Proteoglycans in cancer     112920632 (WNT9B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112920632 (WNT9B)    05226 Gastric cancer     112920632 (WNT9B)    05217 Basal cell carcinoma     112920632 (WNT9B)    05224 Breast cancer     112920632 (WNT9B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112920632 (WNT9B)    05022 Pathways of neurodegeneration - multiple diseases     112920632 (WNT9B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112920632 (WNT9B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112920632 (WNT9B) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112920632 (WNT9B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112920632 NCBI-ProteinID:  XP_025855233 UniProt:  A0A3Q7SG22 LinkDB All DBs Position Unknown AA seq 448 aa AA seqDB search MRPEGLHVPPARPPAGAASEQGRLRPPAGPGRAGPRTQTLAAGGPQSRRAAGVRAPARPR LPRPGSGPGAPSGNSLQSKDCVIIQGSSSYRELQGAAANTTYRQYFPDFPHHRSCPSLTG REVLTPFPGLGTATAPAQGGAHLKQCDLLKLSRRQKQLCRREPGLAETLQDAAHLSLLEC QFQFRHERWNCSLEGRTGLLKRGFKETAFLYAVSSAALTHTLARACSAGRMERCTCDDSP GLESRQAWQWGVCGDNLKYSTKFLSNFLGPKRGSKDLRARVDAHNTHVGIKAVKSGLRTT CKCHGVSGSCAVRTCWKQLSPFRETGQALKLRYDSAVKVSSATNEALGRLELWAPVRPGS PAKGLAPRPGDLVYMEDSPSFCRPSKYSPGTAGRVCSREASCSSLCCGRGYDTQSRLVAF SCHCQVQWCCYVECQQCVQEELVYTCKH NT seq 1347 nt NT seq  +upstreamnt  +downstreamnt atgcggcccgagggcctccacgttccgcccgcgcgtcccccggcgggcgccgcgtcagag cagggccgacttcgccctcccgctggccccggccgcgcgggacctcgaactcagacctta gccgccggcgggccgcagtcccggcgcgctgcgggggttcgcgccccagctcggcctcgg ctgccccggcccggctccggcccgggcgccccgtccgggaacagtctccagagcaaagac tgtgtgatcatccaggggagcagcagctacagggagctgcagggggcagcagccaatact acctacaggcagtactttccagacttccctcaccataggagctgcccaagcctgaccggg cgggaggtcctgacccccttcccagggctgggcaccgccacggccccagcacagggtggg gcccacctgaagcagtgtgacctgctgaagctgtcccgccggcagaagcagctctgccgg agggagcccggcctggccgagaccctgcaggacgctgctcacctcagcctgctggagtgc cagttccagttccgacatgagcgttggaactgcagcctggaggggaggacaggcctgctc aagagaggtttcaaggagacggccttcctgtatgcagtgtcctcggccgccctcacccac acgctggcccgggcctgcagtgccgggcgcatggagcgctgcacctgtgatgactctccg ggcctggagagccgacaggcctggcagtggggcgtgtgcggcgacaacctcaagtacagc accaagttcctgagcaacttcctggggcccaagagaggaagcaaagacctgagggcacgg gtggatgctcacaatacccacgtgggcatcaaggcagtaaagagtggcctcaggaccaca tgtaagtgccacggtgtttcgggctcctgcgccgtgcgcacctgctggaagcagctctcc ccgttccgagagacaggccaggcgctaaagctgcgctatgactcagctgtcaaggtgtcc agtgctaccaacgaggccttgggccgcctggagctgtgggcacctgtccggcctggcagc cccgccaaaggcctggccccacggcctggggacctggtctacatggaagactcgcccagt ttctgccggcccagcaagtactcaccaggcacagcgggcagggtgtgttctcgggaggcc agctgcagcagcctgtgctgcgggcggggctatgacacccagagccgcctggtggccttc tcctgccactgccaggtgcagtggtgctgctacgttgagtgccagcagtgcgtgcaggag gagctcgtgtatacctgcaaacactag

Vulpes vulpes (red fox): 112920633 Help Entry 112920633         CDS       T05911                                  Gene name WNT3 Definition (RefSeq) proto-oncogene Wnt-3   KO K00312   wingless-type MMTV integration site family, member 3 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05206   MicroRNAs in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112920633 (WNT3)    04390 Hippo signaling pathway     112920633 (WNT3)    04150 mTOR signaling pathway     112920633 (WNT3)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112920633 (WNT3)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112920633 (WNT3)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112920633 (WNT3)    05206 MicroRNAs in cancer     112920633 (WNT3)    05205 Proteoglycans in cancer     112920633 (WNT3)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112920633 (WNT3)    05226 Gastric cancer     112920633 (WNT3)    05217 Basal cell carcinoma     112920633 (WNT3)    05224 Breast cancer     112920633 (WNT3)   09164 Neurodegenerative disease    05010 Alzheimer disease     112920633 (WNT3)    05022 Pathways of neurodegeneration - multiple diseases     112920633 (WNT3)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112920633 (WNT3)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112920633 (WNT3) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112920633 (WNT3) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112920633 NCBI-ProteinID:  XP_025855234 UniProt:  A0A3Q7S7B0 LinkDB All DBs Position Unknown AA seq 531 aa AA seqDB search MGAAGPTSWSCGEEASVRCQAGCARGTAVALTAGLACGRGGPEGICLGRRRLQSQGLSVL QRRGKERGISLLREVWGATLALAASQCPGLGASAGLGRPTCRGLMRPGSGHPFGVLGQKW PHRVETKRQWGGPHPSASLSTAPKCQRREWKGLRFFPGEPCSPAALSGWRCADHPARTLG SVPAPGIAELLGQPCHRPLSACRSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCRNYIE IMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIASAGVA FAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRPDARS AMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDSASEM VVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTCNVTS HGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECIRIYDVHTCK NT seq 1596 nt NT seq  +upstreamnt  +downstreamnt atgggggcggcagggcccacctcctggagctgtggtgaggaagcatccgtgaggtgccag gccgggtgtgcgagaggaacggctgtcgctctgactgctggccttgcatgtggccgcggg gggccagagggaatctgcttgggtcgaaggagactacagtctcaggggctcagtgtcctt cagaggaggggcaaggaacgaggcatctccctgctgagggaggtttggggagcaactctg gccttggcagccagccagtgcccggggctgggggcttctgctgggctggggaggcccacc tgcagggggctgatgagaccagggagtgggcacccctttggagtgctgggacagaagtgg cctcaccgagtggaaacgaagaggcagtgggggggtccccacccctcggcatccctctcc acggctcctaaatgccagagaagggagtggaaaggcctgcgcttcttcccaggggagccc tgctccccagctgccctctcaggatggcgctgtgccgaccatccagcccgaaccctgggc tccgttccggctccagggattgcagagttgctggggcagccgtgccaccgccctctgtct gcctgcaggtccctggccctgggccagcagtacacatccctgggctcacagcccctgctc tgcggctccatcccaggcctggtccccaagcagctgcgcttctgccggaattacatcgaa atcatgcccagcgtggccgagggagtgaagttgggcatccaggagtgccagcaccagttc cggggccgccgctggaactgcaccaccatagatgatagcctggccatcttcggtcctgtc ctggacaaagccacccgcgagtcggccttcgtgcacgccatcgcctcggccggcgtggcc ttcgccgtcacgcgctcctgcgccgagggcacctccaccatctgcggctgcgactcgcat cacaaggggccgcccggcgagggctggaagtggggcggctgcagcgaggacgccgacttc ggggtgctcgtgtcccgggagttcgcggatgcgcgtgagaacaggccggacgcacgctcg gccatgaacaagcacaacaacgaggcgggccgcacgaccatcctggaccacatgcacctt aaatgcaagtgccacgggctgtcgggcagctgcgaggtcaagacctgctggtgggcccaa cccgacttccgcgctatcggcgacttcctcaaggacaagtacgacagtgcctcggagatg gtggtggagaagcaccgtgaatcccgtggctgggtggagaccctccgcgccaagtacgcg ctgttcaagccgcccaccgagagggacctggtctactatgagaactcccccaacttctgc gagcccaatcccgagacgggctcctttggcaccagggaccggacttgcaatgtcacctct cacggcatcgatggctgcgacctgctgtgctgtggccgtggccacaacacgaggacggag aagcggaaggagaaatgccactgcatcttccactggtgctgctacgtgagctgccaggag tgcatccgcatctacgacgtgcacacctgcaagtag

Vulpes vulpes (red fox): 112921097 Help Entry 112921097         CDS       T05911                                  Gene name WNT10B Definition (RefSeq) protein Wnt-10b   KO K01357   wingless-type MMTV integration site family, member 10 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112921097 (WNT10B)    04390 Hippo signaling pathway     112921097 (WNT10B)    04150 mTOR signaling pathway     112921097 (WNT10B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112921097 (WNT10B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112921097 (WNT10B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112921097 (WNT10B)    05205 Proteoglycans in cancer     112921097 (WNT10B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112921097 (WNT10B)    05226 Gastric cancer     112921097 (WNT10B)    05217 Basal cell carcinoma     112921097 (WNT10B)    05224 Breast cancer     112921097 (WNT10B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112921097 (WNT10B)    05022 Pathways of neurodegeneration - multiple diseases     112921097 (WNT10B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112921097 (WNT10B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112921097 (WNT10B) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112921097 (WNT10B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112921097 NCBI-ProteinID:  XP_025856017 UniProt:  A0A3Q7T6P6 LinkDB All DBs Position Unknown AA seq 389 aa AA seqDB search MPEEPRPRPPPSGFAGLLLLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG LCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS FSMLAAGVMHAVATACSLGRLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSP GPGSVPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR PRRLSGELVYFEKSPDFCERDPTVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNMLRQTR VERCHCRFHWCCYVLCDECKVTEWVNVCK NT seq 1170 nt NT seq  +upstreamnt  +downstreamnt atgccggaggagccccggccgcggcctccgccctcgggcttcgcgggtctcctgctcctg gcgctgtgcagtcgggccctcagcaatgagatcctgggcctgaagctgcccggggagccg ccgctgaccgccaacaccgtgtgcctgacgctgtcgggcctgagcaagcggcagctgggc ctctgcctgcgcagccccgacgtgacggcatccgcgctgcagggcctgcacatcgcggtc cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcggcgctcgagggcggc ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgtgagagtgctttttcc ttctccatgctggcggcaggggtcatgcacgcggtcgccacggcctgcagcctgggcagg ctagtgagctgcggctgcggctggaagggcagtggtgagcaggaccggctgagggccaag ctgctgcagctgcaggctctgtcccggggcaagagtttcccccactccctgcccagccct ggccccggctcagttcccagccctggcccccaggacacatgggaatggggtggctgtaac catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc cgggacatccaggcaagaatgcgaatccacaacaacagggtggggcgacaggtggtaact gaaaacctgaagcggaaatgcaagtgccacggcacgtcgggcagctgccagttcaagacg tgctggagggcggccccagagttccgggcagtgggggcagccctgagggagcggctgggt cgggccatcttcatcgatacccacaaccgcaactccggagccttccagccccgcctgcgt ccccgccgcctctcaggagagctggtttacttcgagaagtctccggacttctgcgagcga gaccctaccgtgggctcccccggcactcggggccgggcctgcaacaagaccagccggctg ctcgatggctgtggcagcctgtgctgcggccgtgggcacaacatgctccggcagacacga gttgagcgctgtcactgccgcttccactggtgctgctatgtgctgtgcgatgagtgcaag gtcacggagtgggtcaacgtgtgtaagtga

Vulpes vulpes (red fox): 112921098 Help Entry 112921098         CDS       T05911                                  Gene name WNT1 Definition (RefSeq) proto-oncogene Wnt-1 isoform X1   KO K03209   wingless-type MMTV integration site family, member 1 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112921098 (WNT1)    04390 Hippo signaling pathway     112921098 (WNT1)    04150 mTOR signaling pathway     112921098 (WNT1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112921098 (WNT1)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112921098 (WNT1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112921098 (WNT1)    05205 Proteoglycans in cancer     112921098 (WNT1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112921098 (WNT1)    05226 Gastric cancer     112921098 (WNT1)    05217 Basal cell carcinoma     112921098 (WNT1)    05224 Breast cancer     112921098 (WNT1)   09164 Neurodegenerative disease    05010 Alzheimer disease     112921098 (WNT1)    05022 Pathways of neurodegeneration - multiple diseases     112921098 (WNT1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112921098 (WNT1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112921098 (WNT1) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112921098 (WNT1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112921098 NCBI-ProteinID:  XP_025856019 UniProt:  A0A3Q7S8W4 LinkDB All DBs Position Unknown AA seq 370 aa AA seqDB search MGHWALLPGGVSAALLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTASGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRVLHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggcactgggcgctgctgcccggcggggtttctgctgcgctcttgctggcgctggcc gctctgcccgcagccctggccgccaacagcagcggccgatggtggggcatcgtgaacgtc gcctcctccacgaacctgctgaccgactccaagagtctgcaactggtgctcgagcccagt cttcagctgctgagccgcaaacagcggaggctgatccgtcagaacccggggatcctgcac agcgtgagcggggggctgcagagcgctgtgcgagagtgcaagtggcagttccgcaaccgc cgctggaactgccccacggcttcggggccccacctcttcggcaagatcgtcaaccgaggc tgtcgggaaaccgcatttatcttcgccatcacctccgccggggttacccattcagtggca cgctcctgctcagagggctccatcgagtcctgcacgtgcgactaccggcggcgcggcccc gggggccccgactggcactgggggggctgcagcgacaacatcgacttcggccgcctcttc ggcagggagtttgtggactccggggagaaggggcgggacctgcgcttcctcatgaacctg cacaacaacgaggcgggccgcacgacggtgttctccgagatgcgccaggagtgcaagtgc cacgggatgtcgggctcgtgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc gccgtgggcgacgtgctgcgcgaccgcttcgatggggcctcgcgcgtcctctacggcaac cgcggcagcaaccgcgcctcccgggcggagctgctgcgcctggagcccgaagaccccgcg cacaagccgccctccccccacgacctcgtctactttgagaaatcgcccaatttctgcacc tacagcggacgcctggggacggcgggcacggcggggcgcgcctgcaacagctcctcgccc gcgctggacggctgcgagctgctctgctgcggccggggccaccgcacgcgcacacagcgc gtcaccgagcgctgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc acgcacacgcgcgtactgcacgagtgtctgtga

Vulpes vulpes (red fox): 112921902 Help Entry 112921902         CDS       T05911                                  Gene name WNT8A Definition (RefSeq) protein Wnt-8a   KO K00714   wingless-type MMTV integration site family, member 8 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112921902 (WNT8A)    04390 Hippo signaling pathway     112921902 (WNT8A)    04150 mTOR signaling pathway     112921902 (WNT8A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112921902 (WNT8A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112921902 (WNT8A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112921902 (WNT8A)    05205 Proteoglycans in cancer     112921902 (WNT8A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112921902 (WNT8A)    05226 Gastric cancer     112921902 (WNT8A)    05217 Basal cell carcinoma     112921902 (WNT8A)    05224 Breast cancer     112921902 (WNT8A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112921902 (WNT8A)    05022 Pathways of neurodegeneration - multiple diseases     112921902 (WNT8A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112921902 (WNT8A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112921902 (WNT8A) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112921902 (WNT8A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112921902 NCBI-ProteinID:  XP_025857082 UniProt:  A0A3Q7T8N8 LinkDB All DBs Position Unknown AA seq 352 aa AA seqDB search MGDLFMLRVAVGICYATFSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW ERWNCPESALQLSTHNRLRSATRETSFIHAISSAGVMYIITKNCSMGDFENCGCDESKNG KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRAIMKRTC KCHGISGSCSIQTCWLQLADFREMGDYLKAKYKQALKIEMDKRQLRAGNSAEGHWAPTEA FLPSAEAELIFLEESPDYCTRNSSLGIYGTEGRECLQDSHNTSRWEQHSCGRLCTECGLQ VEERRTEAISSCNCKFQWCCTVRCDQCRHVVNKYYCTSSLGSALARGKGSAS NT seq 1059 nt NT seq  +upstreamnt  +downstreamnt atgggggacctgtttatgctcagggtggccgtgggcatatgctacgccaccttcagtgcc tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctatctgacctacacc accagcgtggccctgggcgcccagagtggcatagaggagtgtaaattccaatttgcttgg gaacgctggaactgcccggaaagtgctctccagctctccactcacaacaggctgagaagt gccaccagggagacttctttcattcatgccatcagctctgctggagtcatgtacatcatc accaagaactgcagcatgggcgactttgaaaactgtggctgtgatgagtcaaaaaacgga aaaacaggaggtcacggctggatctggggaggctgcagcgacaatgtggaatttggggaa aggatctccaaactctttgtggatagcctggaaaagggaaaagatgcgagagccctgatg aaccttcacaacaacagggcaggcaggctggcagtgagagccatcatgaaaaggacctgc aaatgtcatggcatctctgggagctgcagcatccaaacatgctggctgcagctggctgac ttccgggaaatgggagactacctgaaagccaagtacaagcaggccctgaaaattgagatg gataagcggcagttgagggctgggaacagtgctgagggccactgggcccccactgaggcc ttccttcctagtgcagaggctgagctgatctttttagaggaatcaccagattactgtacc cgtaattccagtctgggcatctatggcacagaaggccgggagtgtctgcaggacagccac aacacatccaggtgggagcaacacagctgcgggcgcctatgcaccgagtgtggcctgcag gtggaagagagaagaactgaggctatcagcagctgtaactgcaaattccagtggtgctgt acagtcaggtgcgaccagtgtaggcacgtagtgaacaagtactactgcacaagctccctg ggcagcgctttggccagaggcaagggcagtgcttcatag

Vulpes vulpes (red fox): 112922477 Help Entry 112922477         CDS       T05911                                  Gene name WNT10A Definition (RefSeq) protein Wnt-10a   KO K01357   wingless-type MMTV integration site family, member 10 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112922477 (WNT10A)    04390 Hippo signaling pathway     112922477 (WNT10A)    04150 mTOR signaling pathway     112922477 (WNT10A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112922477 (WNT10A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112922477 (WNT10A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112922477 (WNT10A)    05205 Proteoglycans in cancer     112922477 (WNT10A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112922477 (WNT10A)    05226 Gastric cancer     112922477 (WNT10A)    05217 Basal cell carcinoma     112922477 (WNT10A)    05224 Breast cancer     112922477 (WNT10A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112922477 (WNT10A)    05022 Pathways of neurodegeneration - multiple diseases     112922477 (WNT10A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112922477 (WNT10A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112922477 (WNT10A) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112922477 (WNT10A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Ebola_NP Motif Other DBs NCBI-GeneID:  112922477 NCBI-ProteinID:  XP_025857832 UniProt:  A0A3Q7TA10 LinkDB All DBs Position Unknown AA seq 417 aa AA seqDB search MGSTHPCPRLRLRPRPQPRPALCALLFFLLLLAAAVPRSAPNDILGLRLPPEPVLNANTV CLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKIPYES PIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLKACGCDASRRGDEEAFRRKLHRLQLD ALQRGKGLSHGVPEHPALPPASPGLQDSWEWGGCSPDVGFGERFSKDFLDSREPHRDIHA RMRLHNNRVGRQAVMENMRRKCKCHGTSGSCQLKTCWQVTPEFRAVGALLRSRFHRATLI RPHNRNGGQLEPGPAGAPSPAPGAPGPRRRASPADLVYFEKSPDFCEREPRLDSAGTVGR LCNKSSAGPDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK NT seq 1254 nt NT seq  +upstreamnt  +downstreamnt atgggcagcacccacccttgcccccggctgcggctccgacctcggccccagccgcggccc gcgctctgcgcgctcctgttcttcctactgctgctggctgccgccgtgcccaggtctgca cccaacgacattctgggcctccgcctccccccggagcctgtgctcaatgccaacacggtg tgcctaacgttgccgggcctgagcaggaggcagatggaagtgtgtgtgcgccacccagac gtggctgcctcagccatccagggcatccagatcgccatccatgagtgccagcaccagttc cgggaccagcgctggaactgctccagtctggagactcgcaacaagatcccctacgagagt cccatcttcagcagaggttttcgcgagagcgccttcgcctatgccatcgcggcagctggg gtcgtgcatgccgtgtccaatgcctgtgccctaggcaaactgaaggcctgcggctgcgat gcctcccggcgcggggacgaggaggccttccgccggaagctgcaccgcctgcagctggac gcgctgcagcgtggtaagggcttgagccatggggtcccagaacacccggccctgccccct gccagccccggcctgcaggactcctgggagtggggcggctgtagccccgacgtgggcttc ggggagcgcttctctaaggactttctggactcccgggagcctcacagagacatccacgca cgcatgagactccacaacaaccgagttgggagacaggcggtgatggagaacatgcggcgg aagtgcaagtgccacggcacgtcgggcagctgccagctcaagacgtgctggcaggtgacg ccggagttccgcgcggtgggggcgctgctgcgcagccgcttccaccgcgccacgctcatc cggccgcacaaccgcaacggcggccagctggagcccggccccgcgggggcgccctcgccg gcccccggcgcccccggcccgcggcgccgcgccagccccgccgacctggtctacttcgag aagtcgcccgacttctgcgagcgcgagccgcgcctggactcggcgggcaccgtgggccgc ctgtgcaacaagagcagcgcgggccccgacggctgcggcagcatgtgctgcggccgcggc cacaacatcctgcgccagacgcgcagcgagcgctgccactgccgcttccactggtgctgc ttcgtggtgtgcgaggagtgccgcatcaccgagtgggtcagcgtgtgcaagtga

Vulpes vulpes (red fox): 112922542 Help Entry 112922542         CDS       T05911                                  Gene name WNT6 Definition (RefSeq) protein Wnt-6   KO K00445   wingless-type MMTV integration site family, member 6 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112922542 (WNT6)    04390 Hippo signaling pathway     112922542 (WNT6)    04150 mTOR signaling pathway     112922542 (WNT6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112922542 (WNT6)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112922542 (WNT6)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112922542 (WNT6)    05205 Proteoglycans in cancer     112922542 (WNT6)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112922542 (WNT6)    05226 Gastric cancer     112922542 (WNT6)    05217 Basal cell carcinoma     112922542 (WNT6)    05224 Breast cancer     112922542 (WNT6)   09164 Neurodegenerative disease    05010 Alzheimer disease     112922542 (WNT6)    05022 Pathways of neurodegeneration - multiple diseases     112922542 (WNT6)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112922542 (WNT6)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112922542 (WNT6) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112922542 (WNT6) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112922542 NCBI-ProteinID:  XP_025857927 UniProt:  A0A3Q7TA64 LinkDB All DBs Position Unknown AA seq 365 aa AA seqDB search MLPPAPSLLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPSGSPDGSATWEWGGCGDDVDFGD EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE LSLCL NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atgctgccgcccgcgccctccctgctcgggctgctgctgctgctgctcctgtgccccgcg cacgtcggtggactgtggtgggcggtgggcagccccctggtcatggaccctaccagcatc tgcaggaaagcgcggcggctggcagggcggcaggctgagctgtgccaggctgagccagaa gtggtggcggagctagcccggggcgcccggcttggggtgcgagagtgccagttccagttc cgtttccgccgctggaactgttccagccacagcaaggccttcgggcgcatcctgcagcag gacatccgggagacggcctttgtgtttgccatcacggctgcgggcgccagccacgcagtc acccaggcctgctccatgggggagctgctgcagtgcggctgccaggcgccccgcggccgg gccccgcccaggccccctggcctgcctggcaccccggggcccccggggccctccggctcc cccgatggcagcgccacctgggagtggggaggctgtggcgacgacgtggacttcggggac gagaaatcaaggctctttatggatgcccggcacaagcggggtcgtggagacatccgtgca ttggtgcaacttcacaacaatgaggcaggccgtctggccgtgcggagccacacgcgcacc gagtgcaagtgccacggactgtcgggctcgtgcgcgctgcgaacctgctggcagaagctg cccccgttccgcgaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgcgtc atgggaaccaacgacggcaaggccctgctgcccgccgtccgcaccctgaagccgccgggc cgcgccgacctcctctacgccgccgactcgcccgacttctgcgcgcccaaccggcgcacc ggctctccgggcacgcgaggccgcgcgtgcaacagcagcgccccggacctcagcggctgc gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaggagaactgc ctgtgccgcttccactggtgctgcgtcgtgcagtgccaccgctgccgcgtgcgcaaggag ctcagcctctgcctctga

Vulpes vulpes (red fox): 112928634 Help Entry 112928634         CDS       T05911                                  Gene name WNT11 Definition (RefSeq) protein Wnt-11   KO K01384   wingless-type MMTV integration site family, member 11 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112928634 (WNT11)    04390 Hippo signaling pathway     112928634 (WNT11)    04150 mTOR signaling pathway     112928634 (WNT11)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112928634 (WNT11)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112928634 (WNT11)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112928634 (WNT11)    05205 Proteoglycans in cancer     112928634 (WNT11)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112928634 (WNT11)    05226 Gastric cancer     112928634 (WNT11)    05217 Basal cell carcinoma     112928634 (WNT11)    05224 Breast cancer     112928634 (WNT11)   09164 Neurodegenerative disease    05010 Alzheimer disease     112928634 (WNT11)    05022 Pathways of neurodegeneration - multiple diseases     112928634 (WNT11)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112928634 (WNT11)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112928634 (WNT11) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112928634 (WNT11) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112928634 NCBI-ProteinID:  XP_025866236 UniProt:  A0A3Q7TLQ1 LinkDB All DBs Position Unknown AA seq 354 aa AA seqDB search MRARPRVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR SNLELMHTIVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVAADLKTR YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK NT seq 1065 nt NT seq  +upstreamnt  +downstreamnt atgagggcgcggccgcgggtgtgcgaggcgctcctcttcgccctggcgctccagaccggc gtgtgctacggcatcaaatggctggcgctgtccaagaccccggcggccctggcgctgaac cagacgcagcactgcaagcagctggaggggctggtgtctgcgcaggtgcagctctgccgc agcaacctggagcttatgcacaccatcgtgcacgctgcccgcgaggtcatgaaggcctgc cgcagggcctttgcggacatgcgctggaactgctcctccatcgagcttgcccccaactac ctgcttgacctggagagagggacccgggagtcggccttcgtgtatgcgctgtcggcggcc gccatcagccacgccatcgcccgggcctgcacctccggggacctgcccggctgctcctgc ggccccgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac ctcagctacgggcttctcatgggagccaagttttccgatgctcctatgaaggtgaaaaaa acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct ctgcgcgcctctctggaaatgaagtgtaagtgccatggggtatctggctcctgctccatc cgcacctgctggaaggggctgcaggagcttcgagatgtggctgccgacctcaagacccgc tacctgtcggccaccaaggtggtgcaccgccccatgggcacccgcaagcacctggtgccc aaggacctggacatcaggcctgtgaaggactcagagcttgtctatctgcagagttcgccc gacttctgcatgaagaacgagaaggtgggctcccacgggacgcaagacaggcagtgcaac aaaacatcccatggcagtgacagctgtgacctcatgtgctgcggccgtggctacaacccg tacacagaccgcgtggtcgagcgctgccactgcaagtatcactggtgctgctacgttacc tgccgccgctgcgagcgcacagtggagcgctacgtttgcaagtga

Vulpes vulpes (red fox): 112929848 Help Entry 112929848         CDS       T05911                                  Gene name WNT4 Definition (RefSeq) protein Wnt-4 isoform X1   KO K00408   wingless-type MMTV integration site family, member 4 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04360   Axon guidance vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04919   Thyroid hormone signaling pathway vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112929848 (WNT4)    04390 Hippo signaling pathway     112929848 (WNT4)    04150 mTOR signaling pathway     112929848 (WNT4)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112929848 (WNT4)  09150 Organismal Systems   09152 Endocrine system    04919 Thyroid hormone signaling pathway     112929848 (WNT4)    04916 Melanogenesis     112929848 (WNT4)   09158 Development and regeneration    04360 Axon guidance     112929848 (WNT4)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112929848 (WNT4)    05205 Proteoglycans in cancer     112929848 (WNT4)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112929848 (WNT4)    05226 Gastric cancer     112929848 (WNT4)    05217 Basal cell carcinoma     112929848 (WNT4)    05224 Breast cancer     112929848 (WNT4)   09164 Neurodegenerative disease    05010 Alzheimer disease     112929848 (WNT4)    05022 Pathways of neurodegeneration - multiple diseases     112929848 (WNT4)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112929848 (WNT4)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112929848 (WNT4) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112929848 (WNT4) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt MEF2_binding Motif Other DBs NCBI-GeneID:  112929848 NCBI-ProteinID:  XP_025867920 UniProt:  A0A3Q7UKT0 LinkDB All DBs Position Unknown AA seq 360 aa AA seqDB search MRRFPEPWAGHSLGLAVEGGGRSTARRSTPRPLPRYLAKLSSVGSISEEETCEKLKGLIQ RQVQMCKRNLEVMDSVRRGAQLAIEECQYQFRNRRWNCSTLDSLPVFGKVVTQGTREAAF VYAISSAGVAFAVTRACSSGELEKCGCDRTVHGVSPQGFQWSGCSDNIAYGVAFSQSFVD VRERSKGASSSRALMNLHNNEAGRKAILTHMRVECKCHGVSGSCEVKTCWRAVPPFRQVG HALKEKFDGATEVEPRRVGSSRALVPRNAQFKPHTDEDLVYLEPSPDFCEQDMRSGVLGT RGRTCNKTSKAIDGCELLCCGRGFHTAQVELAERCSCKFHWCCFVKCRQCQRLVELHTCR NT seq 1083 nt NT seq  +upstreamnt  +downstreamnt atgaggcggttcccagagccctgggctgggcacagcctgggcctggcagtggaaggagga ggaaggagcactgcacggcgttccaccccccgccctctccccaggtacctggccaagctg tcctcggtggggagcatctcggaggaggagacgtgcgagaagctcaagggcctgatccag aggcaggtgcagatgtgtaagcggaacctggaggtgatggactcggtgcgccggggcgcc cagctggccatcgaggagtgccagtaccagttccggaaccggcgctggaactgctccacg ctcgactccctgcccgtcttcggcaaggtggtgacgcaagggactcgggaggcggccttc gtgtacgccatctcgtcagcaggtgtggccttcgccgtgacgcgggcgtgcagcagtggg gagctggagaagtgcggctgtgaccggacggtgcacggggtcagcccgcagggcttccag tggtcggggtgctcggacaacatcgcctacggcgtggccttctcccagtccttcgtggac gtgcgggagagaagcaagggggcctcgtccagccgcgccctcatgaacctccacaacaac gaggctggcaggaaggctatcctgacacacatgcgggtggagtgcaagtgccacggggtg tcgggctcctgtgaggtaaagacgtgctggcgagccgtgccgcccttccgccaggtgggc cacgcactgaaggagaagttcgatggcgccaccgaggtggagccgcgccgtgtgggctcc tccagggcactggtgccacgcaacgcacagttcaagccgcacacggacgaggacctggta tatttggagcccagcccggacttctgcgagcaggacatgcgcagcggcgtgctgggcacg cggggccgcacgtgcaacaagacgtccaaggccatcgacggctgtgagctgctgtgctgt ggccgcggcttccacacggcgcaggtggagctggccgagcgctgcagctgcaagttccac tggtgctgcttcgtcaagtgccggcagtgccagcggctggtggagctgcacacgtgccgg tga

Vulpes vulpes (red fox): 112929869 Help Entry 112929869         CDS       T05911                                  Gene name WNT2 Definition (RefSeq) protein Wnt-2   KO K00182   wingless-type MMTV integration site family, member 2 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112929869 (WNT2)    04390 Hippo signaling pathway     112929869 (WNT2)    04150 mTOR signaling pathway     112929869 (WNT2)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112929869 (WNT2)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112929869 (WNT2)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112929869 (WNT2)    05205 Proteoglycans in cancer     112929869 (WNT2)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112929869 (WNT2)    05226 Gastric cancer     112929869 (WNT2)    05217 Basal cell carcinoma     112929869 (WNT2)    05224 Breast cancer     112929869 (WNT2)   09164 Neurodegenerative disease    05010 Alzheimer disease     112929869 (WNT2)    05022 Pathways of neurodegeneration - multiple diseases     112929869 (WNT2)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112929869 (WNT2)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112929869 (WNT2) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112929869 (WNT2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112929869 NCBI-ProteinID:  XP_025867930 UniProt:  A0A3Q7UKU0 LinkDB All DBs Position Unknown AA seq 360 aa AA seqDB search MNAPVGGTGLWLPLLLAWLAPGVGASWWYMRATGGSSRVMCDNVPGLVSRQRQLCHRHPD VMRAIGLGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAVSSAGVV FAITRACSQGELKSCSCDPKKKGTAKDSKGSFDWGGCSDNIDYGIKFARAFVDAKERKGK DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDRDAGSPGTAGRVCNLTSRG MDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPTSADWAAPT NT seq 1083 nt NT seq  +upstreamnt  +downstreamnt atgaacgcccctgtcggtggaaccgggctctggctccccctgctcctggcctggctcgcc cccggggtcggcgcctcgtggtggtacatgagagctacaggcggctcctccagggtgatg tgtgacaatgtgccaggcctggtgagccgccagcgccagctgtgccaccgacacccggac gtgatgcgtgccattggcctgggcgtggccgagtggacagcagagtgccagcaccagttc cgccagcaccgctggaactgcaacacgctggacagggatcacagcctctttggcagggtc ctgctccgaagtagtcgggaatctgcctttgtttacgccgtctcctcagctggagttgtg tttgccatcaccagggcctgtagccaaggagagttaaaatcctgttcctgtgatccaaag aagaagggaaccgccaaggacagcaagggcagtttcgactggggtggctgcagcgataac attgactatgggatcaaatttgcccgagccttcgtggatgccaaggaaaggaagggaaag gatgccagagccctgatgaaccttcacaacaacagagccggccggaaggcggtgaagcgg ttcttgaagcaggaatgcaagtgtcacggcgtgagcggctcgtgtacgctgaggacatgc tggctggccatggcggacttcagaaaaacgggcgattacctctggaggaagtacaacggg gccatccaggtcgtcatgaaccaggatggcacggggttcacggtggctaacaagaggttc aagaagccaaccaaaaatgacctcgtgtattttgagaattctccagactattgtatcagg gaccgagacgcaggctccccggggacggcgggccgcgtgtgcaacctgacttcccgcggc atggacagctgcgaggtcatgtgctgcgggagaggctacgacacgtcccgcgtcacgcgg atgaccaagtgcgagtgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg gaggccctagacgtgcacacatgcaaggcccccacgagcgccgactgggcggctcccaca tga

Vulpes vulpes (red fox): 112935842 Help Entry 112935842         CDS       T05911                                  Gene name WNT7B Definition (RefSeq) protein Wnt-7b isoform X1   KO K00572   wingless-type MMTV integration site family, member 7 Organism vvp  Vulpes vulpes (red fox) Pathway vvp04150   mTOR signaling pathway vvp04310   Wnt signaling pathway vvp04390   Hippo signaling pathway vvp04550   Signaling pathways regulating pluripotency of stem cells vvp04916   Melanogenesis vvp04934   Cushing syndrome vvp05010   Alzheimer disease vvp05022   Pathways of neurodegeneration - multiple diseases vvp05165   Human papillomavirus infection vvp05200   Pathways in cancer vvp05205   Proteoglycans in cancer vvp05217   Basal cell carcinoma vvp05224   Breast cancer vvp05225   Hepatocellular carcinoma vvp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:vvp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112935842 (WNT7B)    04390 Hippo signaling pathway     112935842 (WNT7B)    04150 mTOR signaling pathway     112935842 (WNT7B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112935842 (WNT7B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112935842 (WNT7B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112935842 (WNT7B)    05205 Proteoglycans in cancer     112935842 (WNT7B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112935842 (WNT7B)    05226 Gastric cancer     112935842 (WNT7B)    05217 Basal cell carcinoma     112935842 (WNT7B)    05224 Breast cancer     112935842 (WNT7B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112935842 (WNT7B)    05022 Pathways of neurodegeneration - multiple diseases     112935842 (WNT7B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112935842 (WNT7B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112935842 (WNT7B) Glycosaminoglycan binding proteins [BR:vvp00536]  Heparan sulfate / Heparin   Morphogens    112935842 (WNT7B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112935842 NCBI-ProteinID:  XP_025875562 UniProt:  A0A3Q7UQQ4 LinkDB All DBs Position Unknown AA seq 356 aa AA seqDB search MAQPPSLDHAQKLSQVDFLRVSLLWRPLREARSAVIRCGPGSQHHLQQDSWLGPAAARHL PEPARCHHRDRGGGTDGHQRVPVPVPLRTLELLRPRREDCLRARAPRSREAAFTYAITAA GVAHAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIK KNARRLMNLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHMLKEKYN AAVQVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRL CNRTSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK NT seq 1071 nt NT seq  +upstreamnt  +downstreamnt atggcgcagcccccctccctggatcatgcacagaaactttcgcaagtggattttctacgt gtttctctgctttggcgtcctctacgtgaagctcggagcgctgtcatccgttgtggccct gggagccaacatcatctgcaacaagattcctggcttggccccgcggcagcgcgccatctg ccagagccggcccgatgccatcatcgtgatcggggagggggcacagatgggcatcaacga gtgccagtaccagttccgcttcggacgctggaactgctccgccctcggcgagaagactgt cttcgggcaagagctccgaggagccgcgaggcggccttcacctacgccatcactgcggcc ggggtggcccatgccgtgacggccgcctgcagccagggtaacctgagcaactgcggctgt gaccgcgagaagcagggctactacaaccaggccgagggctggaagtggggtggctgctcc gccgacgtgcgctacggcatcgacttctcccggcgcttcgtggacgcccgtgagatcaag aagaacgcgcggcgcctcatgaacctgcacaacaacgaggccggcaggaaggtcctggag gagcgcatgaagctggagtgcaagtgccacggcgtgtcgggctcatgcaccaccaagacg tgctggaccacgctgcccaagttccgcgaggtgggccacatgctgaaggagaagtacaac gcggcggtgcaggtggaggtggtgcgggccagccgcctgcggcagcccaccttcctgcgc atcaagcagctgcgcagctaccagaagcccatggagacggacctggtgtacatcgagaag tcgcccaactactgcgaggaggacgcggccacgggcagtgtgggcacgcagggccgcctg tgcaaccgcacgtcgccgggcgcggatggctgcgacaccatgtgctgcggccgaggctac aacacgcaccagtacaccaaggtgtggcagtgcaactgcaagttccactggtgctgcttc gtcaagtgtaacacctgcagcgagcgcaccgaggtcttcacctgcaagtga

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