Puma concolor (puma): 112867060 Help Entry 112867060         CDS       T08890                                  Symbol WNT10A Name (RefSeq) protein Wnt-10a   KO K01357   wingless-type MMTV integration site family, member 10 Organism pcoo  Puma concolor (puma) Pathway pcoo04150   mTOR signaling pathway pcoo04310   Wnt signaling pathway pcoo04390   Hippo signaling pathway pcoo04519   Cadherin signaling 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     112867060 (WNT10A)    04390 Hippo signaling pathway     112867060 (WNT10A)    04150 mTOR signaling pathway     112867060 (WNT10A)   09133 Signaling molecules and interaction    04519 Cadherin signaling     112867060 (WNT10A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     112867060 (WNT10A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     112867060 (WNT10A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     112867060 (WNT10A)    05205 Proteoglycans in cancer     112867060 (WNT10A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     112867060 (WNT10A)    05226 Gastric cancer     112867060 (WNT10A)    05217 Basal cell carcinoma     112867060 (WNT10A)    05224 Breast cancer     112867060 (WNT10A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     112867060 (WNT10A)   09164 Neurodegenerative disease    05010 Alzheimer disease     112867060 (WNT10A)    05022 Pathways of neurodegeneration - multiple diseases     112867060 (WNT10A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     112867060 (WNT10A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pcoo00536]     112867060 (WNT10A) Glycosaminoglycan binding proteins [BR:pcoo00536]  Heparan sulfate / Heparin   Morphogens    112867060 (WNT10A) SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  112867060 NCBI-ProteinID:  XP_025785829 UniProt:  A0A6P6IDP5 LinkDB All DBs Position Unknown AA seq 382 aa AA seqDB search MKGSKETHGPAWAKLLGFQTVSDLWADPDLGADACVPVSIARSWSAPNDILGLRLPPEPV LNANTVCLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRN KIPYESPIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLRACGCDASRRGDEEAFRRKL HRLQLDALQRGKGLSHGVPEHPALPPASPGLQDSWEWGGCSPDVGFGERFSKDFLDSREP HRDIHARMRLHNNRVGSRFHRATLIRPHNRNGGQLEPGPAGAPSPAPGVPGPRRRASPAD LVYFEKSPDFCEREPRLDSAGTVGRLCNKSSAGPDGCGSMCCGRGHNILRQTRSERCHCR FHWCCFVVCEECRITEWVSVCK NT seq 1149 nt NT seq  +upstreamnt  +downstreamnt atgaaaggaagcaaggagacccacggaccagcttgggccaagctgctagggttccagact gtctcggacctctgggctgacccagacctaggggcggacgcctgcgtcccagtgtctatt gccaggtcttggtctgcacccaacgacattctgggcctccgcctccccccggagcctgtg ctcaatgccaacacggtatgcctaacgttgccgggcctgagtaggcggcagatggaagtg tgtgtgcgccaccccgacgtggccgcctcagccatccagggcatccagatcgccatccac gagtgccagcaccagttccgggaccagcgctggaactgctctagtctcgagactcgaaac aagatcccctacgagagtcccatcttcagcagaggtttccgagagagtgccttcgcctac gccatcgccgcagcgggcgtagtgcacgcggtgtccaatgcctgcgccctgggcaaactg agggcctgcggctgcgacgcctctcggcgcggggacgaggaggccttccgtcggaagctg caccgcctgcagctggacgcgctgcagcgcggtaagggcctgagccacggggtcccggaa cacccagccctgccccctgccagcccgggcctgcaggactcctgggagtggggcggctgt agccccgatgtgggcttcggggagcgcttctcgaaggactttctggactcccgggagcct cacagagacatccacgcacgcatgaggctccacaacaaccgagttgggagccgcttccac cgcgccacgctcatccggccgcacaaccgcaacggtggccagctggagcccggccccgcg ggggccccctcgccagccccgggcgtcccggggccgcggcgccgggccagccccgccgac ctggtctacttcgagaagtcgcccgacttctgcgagcgcgagccgcgcctggactcggcg ggcaccgtgggccgcctgtgcaacaagagcagcgcgggccccgacggctgcggtagcatg tgctgcggccgcggccacaacatcctgcgccagacgcgcagcgagcgctgccactgccgc ttccactggtgctgcttcgtggtctgcgaggagtgccgcatcaccgagtgggtcagcgtc tgcaagtga

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