Panthera tigris altaica (Amur tiger): 102961987 Help Entry 102961987         CDS       T02988                                  Symbol WNT10B Name (RefSeq) Wnt family member 10B   KO K01357   wingless-type MMTV integration site family, member 10 Organism ptg  Panthera tigris altaica (Amur tiger) Pathway ptg04150   mTOR signaling pathway ptg04310   Wnt signaling pathway ptg04390   Hippo signaling pathway ptg04550   Signaling pathways regulating pluripotency of stem cells ptg04916   Melanogenesis ptg04934   Cushing syndrome ptg05010   Alzheimer disease ptg05022   Pathways of neurodegeneration - multiple diseases ptg05165   Human papillomavirus infection ptg05200   Pathways in cancer ptg05205   Proteoglycans in cancer ptg05217   Basal cell carcinoma ptg05224   Breast cancer ptg05225   Hepatocellular carcinoma ptg05226   Gastric cancer Brite KEGG Orthology (KO) [BR:ptg00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     102961987 (WNT10B)    04390 Hippo signaling pathway     102961987 (WNT10B)    04150 mTOR signaling pathway     102961987 (WNT10B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102961987 (WNT10B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     102961987 (WNT10B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102961987 (WNT10B)    05205 Proteoglycans in cancer     102961987 (WNT10B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102961987 (WNT10B)    05226 Gastric cancer     102961987 (WNT10B)    05217 Basal cell carcinoma     102961987 (WNT10B)    05224 Breast cancer     102961987 (WNT10B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102961987 (WNT10B)   09164 Neurodegenerative disease    05010 Alzheimer disease     102961987 (WNT10B)    05022 Pathways of neurodegeneration - multiple diseases     102961987 (WNT10B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102961987 (WNT10B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ptg00536]     102961987 (WNT10B) Glycosaminoglycan binding proteins [BR:ptg00536]  Heparan sulfate / Heparin   Morphogens    102961987 (WNT10B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  102961987 NCBI-ProteinID:  XP_007073141 LinkDB All DBs Position Un AA seq 404 aa AA seqDB search MPEEPRPRPPPSGFAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSHRQLR LCLGRAEAGNKDPDDFEAGEQPPPLCCGGPRWLSPEQIPEVAAYFLPPPPSQLPVNLIPP VTPFLSPGFRESAFSFSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQ ALSRGKSFPHSLPSPGPGSGPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQA RMRIHNNRVGRQVVTENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFI DTHNRKSRAFQPRLRPRRLSGELVYFEKSPDFCERDPAVGSPGTRGRACNKTSRLLDGCG RLCCGRGHNLLRQTRVERCHCRFHWCCYVLCDECKVTEWVNVCK NT seq 1215 nt NT seq  +upstreamnt  +downstreamnt atgccggaggagccccggccgcgccctccgccctcgggcttcgcgggtctcctgtttctg gcgttgtgcagtcgggccctcagcaatgagattctgggcctgaagctgcccggcgagccg ccgctgaccgccaacaccgtatgcttgacgctgtcgggcctgagccaccggcagctaagg ctgtgcctgggccgagcagaggctgggaacaaagaccctgatgactttgaagccggggag cagccccctcctctgtgctgtgggggccccaggtggctctcacctgagcagatcccagag gtggctgcttatttccttccacctcccccctctcagctgcctgtcaaccttatccccccc gtcacaccctttttatccccaggtttccgggagagtgctttttccttctccatgctggct gcaggggtcatgcacgcggtagccacggcctgcagcctgggcaagctggtgagctgcggc tgcggctggaagggcagtggtgagcaggatcggctgagggccaaactactgcagctgcag gcactgtcccggggcaagagtttcccccactccctgcccagtcctggccctggctcaggc cccagccctggcccccaggacacatgggaatggggtggctgtaaccatgacatggacttt ggagagaagttctctcgggatttcttggattccagggaagctccccgggacatccaggca agaatgcgaatccacaacaacagggtggggcgacaggtggtgactgaaaacctgaagcgg aaatgcaagtgccatggcacgtcgggcagttgccagttcaagacctgctggagggcggcc ccagagttccgggcagtgggggcggcgttgagggagcggctgggtcgggccatcttcatc gatacccacaaccgcaaatccagagccttccagccccgcctgcgtccccgtcgcctctca ggagagctggtctactttgagaagtcgcctgacttctgtgagcgagaccctgccgtgggc tccccgggcactcggggccgggcctgcaataagaccagccgcctgctggatggctgtggc aggctgtgctgtggccgtgggcacaacctgctccggcagacacgagtcgagcgctgtcat tgccgcttccactggtgctgctacgtgctgtgtgatgagtgcaaggtcacagagtgggtc aacgtgtgtaagtga

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