Bison bison bison (American bison): 104981617 Help Entry 104981617         CDS       T08726                                  Symbol WNT2B Name (RefSeq) protein Wnt-2b isoform X1   KO K00182   wingless-type MMTV integration site family, member 2 Organism bbis  Bison bison bison (American bison) Pathway bbis04150   mTOR signaling pathway bbis04310   Wnt signaling pathway bbis04390   Hippo signaling pathway bbis04550   Signaling pathways regulating pluripotency of stem cells bbis04916   Melanogenesis bbis04934   Cushing syndrome bbis05010   Alzheimer disease bbis05022   Pathways of neurodegeneration - multiple diseases bbis05165   Human papillomavirus infection bbis05200   Pathways in cancer bbis05205   Proteoglycans in cancer bbis05217   Basal cell carcinoma bbis05224   Breast cancer bbis05225   Hepatocellular carcinoma bbis05226   Gastric cancer Brite KEGG Orthology (KO) [BR:bbis00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     104981617 (WNT2B)    04390 Hippo signaling pathway     104981617 (WNT2B)    04150 mTOR signaling pathway     104981617 (WNT2B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     104981617 (WNT2B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     104981617 (WNT2B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     104981617 (WNT2B)    05205 Proteoglycans in cancer     104981617 (WNT2B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     104981617 (WNT2B)    05226 Gastric cancer     104981617 (WNT2B)    05217 Basal cell carcinoma     104981617 (WNT2B)    05224 Breast cancer     104981617 (WNT2B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     104981617 (WNT2B)   09164 Neurodegenerative disease    05010 Alzheimer disease     104981617 (WNT2B)    05022 Pathways of neurodegeneration - multiple diseases     104981617 (WNT2B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     104981617 (WNT2B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:bbis00536]     104981617 (WNT2B) Glycosaminoglycan binding proteins [BR:bbis00536]  Heparan sulfate / Heparin   Morphogens    104981617 (WNT2B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  104981617 NCBI-ProteinID:  XP_010829105 Ensembl:  ENSBBBG00000010055 UniProt:  A0A6P3GRL9 LinkDB All DBs Position Unknown AA seq 394 aa AA seqDB search MLRPGGAEEAAQLPPRRVSAPVPESAPRPTVPDGSRASARLSLACLLLLLLLLTLPARVD TSWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWN CTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHH DQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLEC KCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRT DLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCEC KFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT NT seq 1185 nt NT seq  +upstreamnt  +downstreamnt atgctgaggccgggtggtgcggaggaagccgcgcagctaccccctcgacgcgttagcgcc cctgtccccgagtccgctcccagacccacggtccccgacggctctcgggcttcggcccgc ctaagtcttgcctgccttctgttgctgctactgctgctgacgctgccggcccgcgtagac acgtcctggtggtacatcggggcactaggggcccgtgtgatctgtgacaatatccctggg ctggtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctccgtgggt gagggtgcccgagagtggatccgagagtgtcagcaccagttccgccatcatcgctggaac tgcaccaccctggaccgggaccacactgtctttggccgtgtcatgctcagaagtagccgg gaggcagcatttgtatacgccatctcatcagcaggggtggtccatgctatcactcgtgcc tgtagccagggtgaactgagtgtgtgcagttgtgacccctatacccgtggccgacaccat gaccaacgtggggactttgactggggtggctgcagtgacaacatacactatggtgttcgc tttgccaaagccttcgtggatgccaaggagaagaggcttaaggatgcccgggctctcatg aacttacataacaatcgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgt aagtgccatggcgtgagtggctcctgtactctgcgcacctgctggcgtgcactctcagat ttccgccgcacaggtgattacctgcggcggcgctatgacggggctgtgcaagtaacggcc acccaggatggcgcaaacttcacggcagctcgccaaggctatcgccgtgctacccggact gacctggtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcc ctaggcactgcaggccgagtctgtagcaagacatctaaagggacagacggttgtgaaatc atgtgctgcggccgagggtatgacacaactcgagttacccgtgtcacccagtgtgagtgc aaattccactggtgctgtgctgtgcggtgcaaggagtgcagaaacactgtggacgtccat acttgcaaggcccccaagaaggcagagtggctggatcagacctga

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