Panthera pardus (leopard): 109249055 Help Entry 109249055         CDS       T06062                                  Symbol WNT1 Name (RefSeq) proto-oncogene Wnt-1   KO K03209   wingless-type MMTV integration site family, member 1 Organism ppad  Panthera pardus (leopard) Pathway ppad04150   mTOR signaling pathway ppad04310   Wnt signaling pathway ppad04390   Hippo signaling pathway 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 ppad05207   Chemical carcinogenesis - receptor activation 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     109249055 (WNT1)    04390 Hippo signaling pathway     109249055 (WNT1)    04150 mTOR signaling pathway     109249055 (WNT1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     109249055 (WNT1)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     109249055 (WNT1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     109249055 (WNT1)    05205 Proteoglycans in cancer     109249055 (WNT1)    05207 Chemical carcinogenesis - receptor activation     109249055 (WNT1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     109249055 (WNT1)    05226 Gastric cancer     109249055 (WNT1)    05217 Basal cell carcinoma     109249055 (WNT1)    05224 Breast cancer     109249055 (WNT1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     109249055 (WNT1)   09164 Neurodegenerative disease    05010 Alzheimer disease     109249055 (WNT1)    05022 Pathways of neurodegeneration - multiple diseases     109249055 (WNT1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     109249055 (WNT1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ppad00536]     109249055 (WNT1) Glycosaminoglycan binding proteins [BR:ppad00536]  Heparan sulfate / Heparin   Morphogens    109249055 (WNT1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  109249055 NCBI-ProteinID:  XP_019274767 Ensembl:  ENSPPRG00000010414 UniProt:  A0A9V1E5Z0 LinkDB All DBs Position Unknown AA seq 370 aa AA seqDB search MGHWALLPGWVSATLWLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTATGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRVLHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggcactgggcgctgctgcccggctgggtttctgctacgctgtggctggcgctggcc gctctgcccgcagccctggccgccaacagcagtggccgatggtggggcatcgtgaacgta gcctcctccacgaacctgctgaccgactccaagagtctacaactggtgctcgagcccagt cttcagctgctgagccgcaaacagaggaggctgatccgccagaacccggggatcctgcac agcgtgagcggggggctgcagagcgctgtgcgagagtgcaagtggcagttccgcaaccgc cgctggaactgccccacggctacggggccccacctcttcggcaagatcgtcaaccgaggc tgtcgggaaacggcgtttattttcgctatcacctccgccggggttacccattcggtggcg cgctcctgctcagagggctccatcgagtcttgcacgtgcgactatcggcggcgcggccct gggggccccgattggcactgggggggctgcagcgacaacatcgacttcggccgcctcttc ggcagggagtttgtggactccggggagaaggggcgggacctgcgctttctcatgaacctt cacaacaacgaggctggccgcacgactgtgttctctgagatgcgccaggagtgcaagtgc cacgggatgtcgggctcgtgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc gccgtgggcgacgtgctgcgcgaccgattcgatggcgcctcgcgcgtcctctatggcaac cgcggcagcaaccgcgcctcgagggcggaactgctgcgcctggagcccgaggacccggcg cacaagccgccctccccccacgacctcgtctacttcgagaaatcgcccaatttctgcacg tacagcggacgcctgggaacggcgggcacggccgggcgcgcctgcaacagctcctcgccc gcgctggacggctgcgagctgctctgctgtggccggggccaccgtacgcgcacacagcgc gtcaccgagcgctgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc acgcacacgcgcgtactgcacgagtgtctgtga

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