Mustela nigripes (black-footed ferret): 132001300 Help Entry 132001300         CDS       T09425                                  Symbol WNT2B Name (RefSeq) protein Wnt-2b isoform X1   KO K00182   wingless-type MMTV integration site family, member 2 Organism mnp  Mustela nigripes (black-footed ferret) Pathway mnp04150   mTOR signaling pathway mnp04310   Wnt signaling pathway mnp04390   Hippo signaling pathway mnp04550   Signaling pathways regulating pluripotency of stem cells mnp04916   Melanogenesis mnp04934   Cushing syndrome mnp05010   Alzheimer disease mnp05022   Pathways of neurodegeneration - multiple diseases mnp05165   Human papillomavirus infection mnp05200   Pathways in cancer mnp05205   Proteoglycans in cancer mnp05217   Basal cell carcinoma mnp05224   Breast cancer mnp05225   Hepatocellular carcinoma mnp05226   Gastric cancer Brite KEGG Orthology (KO) [BR:mnp00001]  09130 Environmental Information Processing   09132 Signal transduction    04310 Wnt signaling pathway     132001300 (WNT2B)    04390 Hippo signaling pathway     132001300 (WNT2B)    04150 mTOR signaling pathway     132001300 (WNT2B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     132001300 (WNT2B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     132001300 (WNT2B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     132001300 (WNT2B)    05205 Proteoglycans in cancer     132001300 (WNT2B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     132001300 (WNT2B)    05226 Gastric cancer     132001300 (WNT2B)    05217 Basal cell carcinoma     132001300 (WNT2B)    05224 Breast cancer     132001300 (WNT2B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     132001300 (WNT2B)   09164 Neurodegenerative disease    05010 Alzheimer disease     132001300 (WNT2B)    05022 Pathways of neurodegeneration - multiple diseases     132001300 (WNT2B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     132001300 (WNT2B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:mnp00536]     132001300 (WNT2B) Glycosaminoglycan binding proteins [BR:mnp00536]  Heparan sulfate / Heparin   Morphogens    132001300 (WNT2B) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  132001300 NCBI-ProteinID:  XP_059231727 LinkDB All DBs Position 14:96384797..96397522 Genome browser AA seq 393 aa AA seqDB search MVKPGSAEEAAQLPLRRTRAPVPALGPGPAAPDGSRASARLGLACMLLLLLLTLPARVDT SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK FHWCCAVRCKECRNTVDIHTCKAPKKAEWLDQT NT seq 1182 nt NT seq  +upstreamnt  +downstreamnt atggtgaagccgggtagtgcggaggaagccgcgcagctcccccttcggcgcacccgtgcc cctgtccccgcgctcgggccaggacccgcggcccccgacggctctcgggcctctgcccgc ctcggtcttgcctgcatgcttctgctgttgctgctgacgctcccggcccgcgtagacaca tcctggtggtacatcggggccctgggggcccgagtgatctgtgacaatattcctggtctg gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcggtgggcgag ggtgcccgagaatggatccgagagtgccagcaccagttccgccaccaccgctggaactgt accacgctggatagggaccacactgtctttggccgtgtcatgctcagaagcagccgggag gcagcatttgtatatgccatctcgtcagcaggggtggtccatgctattacccgcgcctgt agccagggtgaactgagtgtgtgcagctgtgacccctacactcgtggccgacaccatgac caacgtggggattttgactggggtggctgcagtgacaacatccactatggtgttcgcttt gccaaggcctttgtggatgccaaggaaaagaggctcaaggatgcccgggccctcatgaac ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgtaag tgccacggcgtaagcggctcctgtactctgcgaacctgctggcgtgcactctcagacttc cgccgcacaggtgactacctgcggcggcgctatgacggcgctgtgcaggtgacagcaacc caggatggcgccaacttcacagcagcccgccaaggctatcgccgtgccacccggactgac cttgtctacttcgacaactccccagactactgtgtcctggacaaggctgccggttcccta ggcaccgcgggccgtgtctgcagcaagacatctaaagggacagatggttgcgaaatcatg tgctgtggccgagggtatgacacaactcgagtcacccgcgtcacccagtgtgagtgcaag ttccactggtgctgtgcagtgcggtgtaaggagtgcagaaacactgtggacatccacacg tgcaaagcccccaagaaggcagagtggctggaccagacctga

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