Panthera tigris altaica (Amur tiger): 102963336 Help Entry 102963336         CDS       T02988                                  Symbol WNT2B Name (RefSeq) Wnt family member 2B   KO K00182   wingless-type MMTV integration site family, member 2 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     102963336 (WNT2B)    04390 Hippo signaling pathway     102963336 (WNT2B)    04150 mTOR signaling pathway     102963336 (WNT2B)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04550 Signaling pathways regulating pluripotency of stem cells     102963336 (WNT2B)  09150 Organismal Systems   09152 Endocrine system    04916 Melanogenesis     102963336 (WNT2B)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     102963336 (WNT2B)    05205 Proteoglycans in cancer     102963336 (WNT2B)   09162 Cancer: specific types    05225 Hepatocellular carcinoma     102963336 (WNT2B)    05226 Gastric cancer     102963336 (WNT2B)    05217 Basal cell carcinoma     102963336 (WNT2B)    05224 Breast cancer     102963336 (WNT2B)   09172 Infectious disease: viral    05165 Human papillomavirus infection     102963336 (WNT2B)   09164 Neurodegenerative disease    05010 Alzheimer disease     102963336 (WNT2B)    05022 Pathways of neurodegeneration - multiple diseases     102963336 (WNT2B)   09167 Endocrine and metabolic disease    04934 Cushing syndrome     102963336 (WNT2B)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    00536 Glycosaminoglycan binding proteins [BR:ptg00536]     102963336 (WNT2B) Glycosaminoglycan binding proteins [BR:ptg00536]  Heparan sulfate / Heparin   Morphogens    102963336 (WNT2B) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  wnt DUF6973 Motif Other DBs NCBI-GeneID:  102963336 NCBI-ProteinID:  XP_015390435 UniProt:  A0A8C9KG20 LinkDB All DBs Position Un AA seq 299 aa AA seqDB search MRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVH AITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKD ARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGA VQVTATQDGANFTAARQGYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGT DGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT NT seq 900 nt NT seq  +upstreamnt  +downstreamnt atgcgctcggtgggcgagggtgcccgagaatggatccgagagtgtcagcaccagttccgc caccaccgctggaactgcaccacgctggaccgggaccacactgtctttggccgtgtcatg ctcagaagtagccgggaggcagcatttgtatatgccatctcgtctgcaggggtggtccat gctatcactcgtgcctgcagccagggagaactgagtgtgtgcagctgtgacccctacacc cgtggccgacaccatgaccaacgtggggattttgactggggtggctgcagtgacaacatc cattatggtgttcgctttgccaaggcctttgtggatgccaaggaaaagaggcttaaggat gcccgggccctcatgaacttacataacaaccgctgtggtcgcacggctgtgcggcggttt ctgaagctcgagtgtaagtgccatggcgttagtggctcctgtactctgcgcacctgctgg cgtgcactctcagacttccgccgcacaggtgattacctgcggcggcgctatgatggggct gtgcaggtgacagcaacccaggatggcgccaacttcacagcagcccgccaaggttatcgc cgtgccacccggactgaccttgtctactttgacaactccccagactactgtgtcttagac aaggctgcaggttccctaggcactgcgggccgtgtctgtagcaagacatccaaagggacg gatggttgcgaaatcatgtgctgtggccgagggtacgacacaactcgagtcacccgtgtc acccagtgtgagtgcaaattccactggtgctgtgcagtgcggtgcaaggagtgcagaaac actgtggacgtccacacttgcaaggcccccaagaaggcagagtggctggaccagacctga

DBGET integrated database retrieval system