Capra hircus (goat): 102180014 Help Entry 102180014         CDS       T02910                                  Symbol WNT1 Name (RefSeq) proto-oncogene Wnt-1   KO K03209   wingless-type MMTV integration site family, member 1 Organism chx  Capra hircus (goat) Pathway chx04150   mTOR signaling pathway chx04310   Wnt signaling pathway chx04390   Hippo signaling pathway chx04550   Signaling pathways regulating pluripotency of stem cells chx04916   Melanogenesis chx04934   Cushing syndrome chx05010   Alzheimer disease chx05022   Pathways of neurodegeneration - multiple diseases chx05165   Human papillomavirus infection chx05200   Pathways in cancer chx05205   Proteoglycans in cancer chx05207   Chemical carcinogenesis - receptor activation chx05217   Basal cell carcinoma chx05224   Breast cancer chx05225   Hepatocellular carcinoma chx05226   Gastric cancer Brite KEGG Orthology (KO) [BR:chx00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     102180014 (WNT1)    04390 Hippo signaling pathway     102180014 (WNT1)    04150 mTOR signaling pathway     102180014 (WNT1)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102180014 (WNT1)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     102180014 (WNT1)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102180014 (WNT1)    05205 Proteoglycans in cancer     102180014 (WNT1)    05207 Chemical carcinogenesis - receptor activation     102180014 (WNT1)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102180014 (WNT1)    05226 Gastric cancer     102180014 (WNT1)    05217 Basal cell carcinoma     102180014 (WNT1)    05224 Breast cancer     102180014 (WNT1)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102180014 (WNT1)   09164 Neurodegenerative disease    05010 Alzheimer disease     102180014 (WNT1)    05022 Pathways of neurodegeneration - multiple diseases     102180014 (WNT1)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102180014 (WNT1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:chx00536]     102180014 (WNT1) Glycosaminoglycan binding proteins [BR:chx00536]  Heparan sulfate / Heparin   Morphogens    102180014 (WNT1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt Motif Other DBs NCBI-GeneID:  102180014 NCBI-ProteinID:  XP_005680064 UniProt:  A0A452F7P8 LinkDB All DBs Position 5:complement(30473873..30478059) Genome browser AA seq 370 aa AA seqDB search MGHWALLPCWVSAALLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTASGPHLFGKIVNRG CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR AVGDVLRDRFDGASRVLYGNRGNNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC THTRILHECL NT seq 1113 nt NT seq  +upstreamnt  +downstreamnt atggggcactgggcgctgctgccttgctgggtttctgctgcgttgttgctggcgctggcc gctctgcctgcagccctggccgccaacagcagtggccgatggtggggcatcgtgaacgta gcctcctctacgaacctgctgaccgactccaagagtctgcagctggtactcgagcccagt ctgcagctgctgagccgcaagcagcggcggctgatccgccagaacccggggatactgcac agcgtgagcggggggctgcagagcgctgtgcgagagtgcaagtggcagttccggaaccgc cgctggaactgtcccacggcttcggggccccacctcttcggcaagatcgtcaaccgaggc tgtcgggaaacagcatttatcttcgccatcacctcggccggggtcacccactcggtggcg cgctcctgctcagagggctccatcgaatcctgcacgtgcgactatcggcgacgcggtcct gggggccccgattggcactgggggggctgcagcgacaacatcgacttcggccgcctcttc ggccgggagtttgtggactccggagagaaggggcgggaccttcgcttcctcatgaacctt cacaacaatgaggcggggcgcacgaccgtgttctccgagatgcgccaggagtgcaagtgc cacgggatgtcgggctcatgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc gcagtgggcgacgtgctgcgggaccgcttcgacggtgcctcgcgcgtcctctacggcaac cgcggcaacaaccgtgcatcgcgggctgaactgctgcgcctggagccggaggacccggct cacaagcctccctcgccccacgacctcgtctacttcgagaaatcgcccaacttctgcacg tacagcggacgcctgggtaccgcgggcacggcggggcgcgcctgcaatagctcgtcgccc gcgctggatggctgtgagctgctctgctgtggccggggccaccgcacgcgcacgcagcgc gtcaccgagcgctgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc acgcacacgcgcatactgcacgagtgcctgtga

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