Panthera pardus (leopard): 109265051 Help Entry 109265051         CDS       T06062                                  Symbol WNT6 Name (RefSeq) protein Wnt-6   KO K00445   wingless-type MMTV integration site family, member 6 Organism ppad  Panthera pardus (leopard) Pathway ppad04150   mTOR signaling pathway ppad04310   Wnt signaling pathway ppad04390   Hippo signaling pathway ppad04519   Cadherin signaling ppad04550   Signaling pathways regulating pluripotency of stem cells ppad04916   Melanogenesis ppad04934   Cushing syndrome ppad05010   Alzheimer disease ppad05022   Pathways of neurodegeneration - multiple diseases ppad05165   Human papillomavirus infection ppad05200   Pathways in cancer ppad05205   Proteoglycans in cancer ppad05217   Basal cell carcinoma ppad05224   Breast cancer ppad05225   Hepatocellular carcinoma ppad05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ppad00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     109265051 (WNT6)    04390 Hippo signaling pathway     109265051 (WNT6)    04150 mTOR signaling pathway     109265051 (WNT6)   09133 Signaling molecules and interaction    04519 Cadherin signaling     109265051 (WNT6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     109265051 (WNT6)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     109265051 (WNT6)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     109265051 (WNT6)    05205 Proteoglycans in cancer     109265051 (WNT6)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     109265051 (WNT6)    05226 Gastric cancer     109265051 (WNT6)    05217 Basal cell carcinoma     109265051 (WNT6)    05224 Breast cancer     109265051 (WNT6)   09172 Infectious disease: viral    05165 Human papillomavirus infection     109265051 (WNT6)   09164 Neurodegenerative disease    05010 Alzheimer disease     109265051 (WNT6)    05022 Pathways of neurodegeneration - multiple diseases     109265051 (WNT6)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     109265051 (WNT6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ppad00536]     109265051 (WNT6) Glycosaminoglycan binding proteins [BR:ppad00536]  Heparan sulfate / Heparin   Morphogens    109265051 (WNT6) SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  109265051 NCBI-ProteinID:  XP_019301480 Ensembl:  ENSPPRG00000008814 UniProt:  A0A9V1FEY5 LinkDB All DBs Position Unknown AA seq 365 aa AA seqDB search MLPPAPSLLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT GSPGTRGRACNSSALDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE LSLCL NT seq 1098 nt NT seq  +upstreamnt  +downstreamnt atgctgccgcccgcgccctccctcctcgggctgctgctgctgctgctcctgtgtcccgcg cacgtcggcggactgtggtgggcggtgggcagccccttggtcatggatcctaccagcatc tgcaggaaagcgcggcggctggcagggcggcaggctgagttgtgccaggccgagccagag gtggtggcagagctagcccggggcgcccggctgggggtgcgggagtgccagttccagttc cgattccgccgctggaactgctccagccacagcaaggccttcgggcgcatcctgcagcag gacatccgggagacggccttcgtgttcgctataacggccgcgggcgccagccacgccgtc acgcaggcctgctccatgggcgagctgctgcagtgcggctgccaggcgccccgagggcgg gccccgccgcgtcccccgggcctgcccggcacccctgggccccccggccccgccggctcc cccgacggcagcgccgcctgggagtgggggggctgcggcgacgacgtggacttcggggac gagaagtcgaggctctttatggacgcgcggcacaagcggggacgcggagacatccgtgcg ttggtgcaactgcacaacaacgaggccggccggctggccgtacggagccacacgcgcacc gagtgcaagtgccatgggctgtcgggctcgtgcgcgctgcgaacctgctggcagaagctg cccccgttccgggaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgtgtc atgggaaccaacgacggcaaggctctgctgcccgcggtccgcactcttaagccgccgggc cgcgccgacctgctctacgccgccgactcgcccgacttctgcgctcccaaccggcgcacc ggctcgccgggcacgcgcggccgcgcctgcaacagcagtgccctggacctcagcggctgt gacctgctgtgctgcggtcgcgggcaccgccaggagagcgtgcagctcgaggagaactgc ctgtgtcgcttccactggtgctgcgtggtgcagtgccaccgctgccgcgtgcgcaaggag ctcagcctctgcctctga

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