Bison bison bison (American bison): 104983013 Help Entry 104983013         CDS       T08726                                  Symbol WNT9B Name (RefSeq) protein Wnt-9b   KO K01064   wingless-type MMTV integration site family, member 9 Organism bbis  Bison bison bison (American bison) Pathway bbis04150   mTOR signaling pathway bbis04310   Wnt signaling pathway bbis04390   Hippo signaling pathway bbis04519   Cadherin signaling bbis04550   Signaling pathways regulating pluripotency of stem cells bbis04916   Melanogenesis bbis04934   Cushing syndrome bbis05010   Alzheimer disease bbis05022   Pathways of neurodegeneration - multiple diseases bbis05165   Human papillomavirus infection bbis05200   Pathways in cancer bbis05205   Proteoglycans in cancer bbis05217   Basal cell carcinoma bbis05224   Breast cancer bbis05225   Hepatocellular carcinoma bbis05226   Gastric cancer Brite KEGG Orthology (KO) [BR:bbis00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104983013 (WNT9B)    04390 Hippo signaling pathway     104983013 (WNT9B)    04150 mTOR signaling pathway     104983013 (WNT9B)   09133 Signaling molecules and interaction    04519 Cadherin signaling     104983013 (WNT9B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104983013 (WNT9B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104983013 (WNT9B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104983013 (WNT9B)    05205 Proteoglycans in cancer     104983013 (WNT9B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104983013 (WNT9B)    05226 Gastric cancer     104983013 (WNT9B)    05217 Basal cell carcinoma     104983013 (WNT9B)    05224 Breast cancer     104983013 (WNT9B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104983013 (WNT9B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104983013 (WNT9B)    05022 Pathways of neurodegeneration - multiple diseases     104983013 (WNT9B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104983013 (WNT9B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:bbis00536]     104983013 (WNT9B) Glycosaminoglycan binding proteins [BR:bbis00536]  Heparan sulfate / Heparin   Morphogens    104983013 (WNT9B) SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  104983013 NCBI-ProteinID:  XP_010830808 UniProt:  A0A6P3GGN4 LinkDB All DBs Position Unknown AA seq 384 aa AA seqDB search MAVERPAYSRKGLHPGCQIDVYVPPTPRATRVQETADNLNWEKHLMDRLWGHGSLTGREV LTPFPGLGTAAPAQGGAHLKQCDLLKLSRRQKQLCRREPGLAETLQDAAHLSLLECQFQF RHERWNCSLEGRTGLLKRGFKETAFLYAVSAAALTHTLARACSAGRMERCTCDDSPGLES RQAWQWGVCGDNLKYSTKFLNNFLGPKRGSKDLRARADAHNTHVGIKAVKSGLRTTCKCH GVSGSCAVRTCWKQLSPFRDTGQVLKLRYDSAVKVSSASNEALGRLELWAPARPGSPSKG PAPRPGDLVYMEDSPSFCRPSKYSPGTGGRVCSREASCSXXXXXXXYDTQSRLTAFSCHC QVQWCCYVECQQCVREELVYTCKH NT seq 1155 nt NT seq  +upstreamnt  +downstreamnt atggcggtagaaagaccagcatattccagaaaggggctgcatcctggttgccagattgat gtatatgttccacccacaccgagggccaccagggtccaggaaacagcagataacttgaac tgggagaaacatctcatggatcgcctctgggggcatggaagcctgaccgggcgggaggtc ctgacgcccttccctgggctgggcaccgctgccccagcacagggtggggcccacctgaag cagtgtgacctcctgaagttgtcccgccggcagaagcagctctgtcggcgggagccaggc ctggctgagaccctgcaggatgccgcacacctcagcctgctcgagtgccagtttcagttc cggcatgagcgctggaactgcagcctggaggggaggacggggctgctcaagagaggtttc aaggagacggccttcctgtatgcggtgtccgcagctgcccttacgcacactctggcccgg gcctgcagcgctggccgcatggagcggtgcacctgtgatgactccccgggcctcgagagc cggcaagcctggcagtggggtgtgtgtggtgacaacctcaagtatagcaccaagttcctg aacaactttctggggcccaagagaggaagcaaagacctgcgggcgcgggcagacgcccac aacacccacgtgggcatcaaggccgtgaagagtggcctccggaccacgtgtaagtgccac ggcgtgtcaggctcctgtgccgtgcgcacctgctggaagcagctgtccccgttccgcgac acaggccaggtgctgaagctgcgctacgactcagccgtcaaggtgtccagtgccagcaat gaggccttgggccgcctggagctgtgggcaccggccagaccaggcagtcccagcaagggc ccggcgccgcggcctggggacctggtctacatggaggactcgcccagtttctgccggccc agcaagtactcgcctggcacagggggcagggtgtgctcccgcgaggccagctgcagcnnn nnnnnnnnnnnnnnnnnctatgacacccagagccgcctgacggccttctcctgccactgc caggtgcagtggtgctgctacgtggagtgccagcagtgtgtgcgggaggagcttgtatac acctgtaagcactag

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