Puma concolor (puma): 112867516 Help Entry 112867516         CDS       T08890                                  Symbol WNT5B Name (RefSeq) protein Wnt-5b   KO K00444   wingless-type MMTV integration site family, member 5 Organism pcoo  Puma concolor (puma) Pathway pcoo04150   mTOR signaling pathway pcoo04310   Wnt signaling pathway pcoo04360   Axon guidance pcoo04390   Hippo signaling pathway pcoo04550   Signaling pathways regulating pluripotency of stem cells pcoo04916   Melanogenesis pcoo04934   Cushing syndrome pcoo05010   Alzheimer disease pcoo05022   Pathways of neurodegeneration - multiple diseases pcoo05165   Human papillomavirus infection pcoo05200   Pathways in cancer pcoo05205   Proteoglycans in cancer pcoo05217   Basal cell carcinoma pcoo05224   Breast cancer pcoo05225   Hepatocellular carcinoma pcoo05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pcoo00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     112867516 (WNT5B)    04390 Hippo signaling pathway     112867516 (WNT5B)    04150 mTOR signaling pathway     112867516 (WNT5B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112867516 (WNT5B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112867516 (WNT5B)   09158 Development and regeneration    04360 Axon guidance     112867516 (WNT5B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112867516 (WNT5B)    05205 Proteoglycans in cancer     112867516 (WNT5B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112867516 (WNT5B)    05226 Gastric cancer     112867516 (WNT5B)    05217 Basal cell carcinoma     112867516 (WNT5B)    05224 Breast cancer     112867516 (WNT5B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112867516 (WNT5B)   09164 Neurodegenerative disease    05010 Alzheimer disease     112867516 (WNT5B)    05022 Pathways of neurodegeneration - multiple diseases     112867516 (WNT5B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112867516 (WNT5B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pcoo00536]     112867516 (WNT5B) Glycosaminoglycan binding proteins [BR:pcoo00536]  Heparan sulfate / Heparin   Morphogens    112867516 (WNT5B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  112867516 NCBI-ProteinID:  XP_025786293 UniProt:  A0A6P6IH69 LinkDB All DBs Position Unknown AA seq 358 aa AA seqDB search MPSLLLLAAALLSSWAQLPAEASSWWSLAVNPVQRPEVFIIGAQPVCSQLPGLSPGQRKL CQLYQEHMAYIGEGAKTGIKECQYQFRQRRWNCSIVDNTSVFGRVMQIGSRETAFTYAVS AAGVVNAISRACREGELSTCGCSRTARPKDLPRDWLWGGCGDNVEYGYRFAKEFVDARER EKNFAKGSEEQGRVLMNLQNNEAGRRAVYKMADVACKCHGVSGSCSLKTCWLQLAEFRKV GDQLKEKYDSAAAMRITRKGKLELVNSRFNQPTPEDLVYVDPSPDYCLRNETTGSLGTQG RLCNKTSEGMDGCELMCCGRGYDQFKSVQVERCHCKFHWCCFVKCRKCTEIVDQYVCK NT seq 1077 nt NT seq  +upstreamnt  +downstreamnt atgcccagtctgctgctgctcgccgctgcactgctgtccagctgggctcagcttccggcc gaagccagctcctggtggtcattagctgtgaacccggtgcagagacccgaggtgtttatc atcggtgcccagcccgtgtgcagccagcttcccgggctgtcccctggccagagaaagctg tgccaactgtaccaggagcacatggcctacataggggagggagccaagacaggcatcaag gaatgccagtaccagttccggcagaggcgttggaactgcagcatcgtggacaacacgtct gtctttgggagagtcatgcagatagggagccgggagacggccttcacctacgcagtgagc gcggcaggcgtggtgaacgccatcagccgagcttgccgcgagggtgagctctccacgtgt ggctgcagccggacagcgcggcccaaggaccttccccgggactggctgtggggcggctgc ggggacaatgtggaatatggctaccgctttgctaaggagttcgtggatgcccgcgagcgg gagaagaactttgccaaggggtcggaggagcagggccgagtactcatgaacctgcagaac aatgaggcgggtcggagggctgtgtataagatggcagacgtggcctgcaaatgccacggc gtctcagggtcctgcagcctcaagacgtgctggctgcagctggccgagttccgcaaggtg ggggaccagctgaaggagaagtacgacagcgcggccgccatgcgcatcacccgcaaaggc aagctggagctggtcaacagccgcttcaaccagcccaccccggaggacctggtctacgtg gaccccagccctgactactgcctgcgcaacgagaccacaggctccctgggcactcagggc cgcctctgcaacaagacctcggagggcatggacggctgcgagctcatgtgctgtggccgt ggctacgaccagttcaagagtgtccaggtggagcgctgtcactgcaagttccactggtgc tgcttcgtcaagtgcaggaaatgcactgagatcgtcgaccagtacgtgtgtaaatag

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