Puma yagouaroundi (jaguarundi): 121016685 Help Entry 121016685         CDS       T07555                                  Symbol WNT9A Name (RefSeq) protein Wnt-9a isoform X1   KO K01064   wingless-type MMTV integration site family, member 9 Organism pyu  Puma yagouaroundi (jaguarundi) Pathway pyu04150   mTOR signaling pathway pyu04310   Wnt signaling pathway pyu04390   Hippo signaling pathway pyu04550   Signaling pathways regulating pluripotency of stem cells pyu04916   Melanogenesis pyu04934   Cushing syndrome pyu05010   Alzheimer disease pyu05022   Pathways of neurodegeneration - multiple diseases pyu05165   Human papillomavirus infection pyu05200   Pathways in cancer pyu05205   Proteoglycans in cancer pyu05217   Basal cell carcinoma pyu05224   Breast cancer pyu05225   Hepatocellular carcinoma pyu05226   Gastric cancer Brite KEGG Orthology (KO) [BR:pyu00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     121016685 (WNT9A)    04390 Hippo signaling pathway     121016685 (WNT9A)    04150 mTOR signaling pathway     121016685 (WNT9A)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     121016685 (WNT9A)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     121016685 (WNT9A)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     121016685 (WNT9A)    05205 Proteoglycans in cancer     121016685 (WNT9A)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     121016685 (WNT9A)    05226 Gastric cancer     121016685 (WNT9A)    05217 Basal cell carcinoma     121016685 (WNT9A)    05224 Breast cancer     121016685 (WNT9A)   09172 Infectious disease: viral    05165 Human papillomavirus infection     121016685 (WNT9A)   09164 Neurodegenerative disease    05010 Alzheimer disease     121016685 (WNT9A)    05022 Pathways of neurodegeneration - multiple diseases     121016685 (WNT9A)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     121016685 (WNT9A)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:pyu00536]     121016685 (WNT9A) Glycosaminoglycan binding proteins [BR:pyu00536]  Heparan sulfate / Heparin   Morphogens    121016685 (WNT9A) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  121016685 NCBI-ProteinID:  XP_040310338 LinkDB All DBs Position Unknown AA seq 295 aa AA seqDB search MCRRDPGVAETLVEAVSMSALECQYQFRFERWNCTLEGRYRASLLKRGFKETAFLYAISS AGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKD LRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVGKRLKHKYETA LKVGSTTNEATGEAGAISPPRGRAAGTGGSDPLPRTPELVHLDDSPSFCLASRFSPGTAG RRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEVYTCKG NT seq 888 nt NT seq  +upstreamnt  +downstreamnt atgtgccgcagagacccgggggtggccgagacactggtggaggcggtgagcatgagcgca cttgaatgccagtaccagttccggtttgagcgctggaactgtaccttggagggccgctac cgggccagcctgctcaagcgaggcttcaaggagaccgccttcctctacgccatctcctct gccggcctgacgcatgcgctggccaaggcgtgtagcgcgggccgcatggagcgctgcacg tgtgatgaggcccccgacctggagaaccgggaggcctggcagtggggcggctgtggggac aacctcaagtacagcagcaagtttgtcaaggagttcctgggccgccgctcaagcaaggac ctgcgagcccgcgtggacttccacaacaacctcgtgggtgtgaaggtaatcaaggccggg gtggagaccacgtgcaagtgccacggcgtgtcgggctcctgtactgtgcggacgtgctgg cggcagctggcacccttccacgaggtgggcaagcgcctgaaacacaagtacgagacagca ctcaaggtgggcagcaccaccaacgaggccaccggggaggccggcgccatctcgccgcct cggggccgggctgcagggacaggaggcagcgacccgctgccccgcacgccagagcttgtg cacctggacgactcgcccagtttctgcttggccagccgcttctccccgggcactgccggc cgcaggtgccaccgggagaagaactgcgagagcatctgctgtgggcgtggccacaacacc cagagccgggtggtgacacggccctgccagtgccaggtgcgctggtgctgctacgtggag tgcaggcagtgcactcagcgtgaggaggtctacacctgcaagggctga

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