Camelus ferus (Wild Bactrian camel): 102521780 Help Entry 102521780         CDS       T02979                                  Symbol WNT1 Name (RefSeq) proto-oncogene Wnt-1   KO K03209   wingless-type MMTV integration site family, member 1 Organism cfr  Camelus ferus (Wild Bactrian camel) Pathway cfr04150   mTOR signaling pathway cfr04310   Wnt signaling pathway cfr04390   Hippo signaling pathway cfr04550   Signaling pathways regulating pluripotency of stem cells cfr04916   Melanogenesis cfr04934   Cushing syndrome cfr05010   Alzheimer disease cfr05022   Pathways of neurodegeneration - multiple diseases cfr05165   Human papillomavirus infection cfr05200   Pathways in cancer cfr05205   Proteoglycans in cancer cfr05207   Chemical carcinogenesis - receptor activation cfr05217   Basal cell carcinoma cfr05224   Breast cancer cfr05225   Hepatocellular carcinoma cfr05226   Gastric cancer Brite KEGG Orthology (KO) [BR:cfr00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     102521780 (WNT1)    04390 Hippo signaling pathway     102521780 (WNT1)    04150 mTOR signaling pathway     102521780 (WNT1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102521780 (WNT1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102521780 (WNT1)    05205 Proteoglycans in cancer     102521780 (WNT1)    05207 Chemical carcinogenesis - receptor activation     102521780 (WNT1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102521780 (WNT1)    05226 Gastric cancer     102521780 (WNT1)    05217 Basal cell carcinoma     102521780 (WNT1)    05224 Breast cancer     102521780 (WNT1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102521780 (WNT1)   09164 Neurodegenerative disease    05010 Alzheimer disease     102521780 (WNT1)    05022 Pathways of neurodegeneration - multiple diseases     102521780 (WNT1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102521780 (WNT1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:cfr00536]     102521780 (WNT1) Glycosaminoglycan binding proteins [BR:cfr00536]  Heparan sulfate / Heparin   Morphogens    102521780 (WNT1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  102521780 NCBI-ProteinID:  XP_006177741 UniProt:  A0A8B6YAC9 LinkDB All DBs Position 12:14747213..14751855 Genome browser AA seq 370 aa AA seqDB search MGHRALLPGWVSATLLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTASGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRVLHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggcaccgggcgctgctgcccggctgggtttccgctacgctgttgctggcgctggcc gctctccctgcagccctggccgccaacagcagtggccgatggtggggcatcgtgaacgta gcctcctccacgaacctgctgaccgactctaagagcctgcaactggtactcgagcccagc ctgcagctgctgagccgcaaacagcggcggctgatccgccagaaccctgggatcctccac agtgtgagcggggggctgcagagcgctgtgcgagagtgcaagtggcagttccggaaccgc cgctggaactgtcccacggcttcagggccccacctcttcggcaaaatcgtcaaccgaggc tgtcgggaaactgcatttatcttcgccatcacctcagccggggtcacccattcggtggcg cgctcctgctcggagggctccatcgagtcctgcacgtgcgactaccggcggcgcggcccg gggggtcccgattggcactgggggggctgcagcgacaacattgacttcggccgcctcttt ggcagggagtttgtggactccggagagaaggggcgggacctgcgcttcctcatgaacctt cacaacaacgaggcgggccgcacgacggtgttctctgagatgcgccaggagtgtaagtgc cacggcatgtccggctcgtgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc gccgtgggggacgtgctgcgcgaccgcttcgatggcgcctcgcgcgtcctctacggtaac cgcggcagcaaccgcgcctcgcgggctgaactgctgcgcctcgagccggaagacccagcg cacaagccgccctcccctcacgacctcgtctactttgagaaatcgcccaacttctgcaca tacagcggacgcttgggtacagcgggcacggcggggcgcgcctgcaacagctcgtcgccc gcgctggacggctgcgagctgctctgctgtggccggggccaccgcacgcgcacgcagcgc gtcacggagcgctgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc acgcacacgcgcgtcctgcacgagtgcctgtga

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