Homo sapiens (human): 10019 Help Entry 10019             CDS       T01001                                  Symbol SH2B3, IDDM20, LNK Name (RefSeq) SH2B adaptor protein 3   KO K12459   SH2B adaptor protein 1/3 Organism hsa  Homo sapiens (human) Pathway hsa04722   Neurotrophin signaling pathway Disease H00236   Congenital polycythemia H00408   Type 1 diabetes mellitus H01605   Myelofibrosis H01612   Essential thrombocythemia Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09156 Nervous system    04722 Neurotrophin signaling pathway     10019 (SH2B3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Phe_ZIP SH2 PH Motif Other DBs NCBI-GeneID:  10019 NCBI-ProteinID:  NP_005466 OMIM:  605093 HGNC:  29605 Ensembl:  ENSG00000111252 Pharos:  Q9UQQ2(Tbio) UniProt:  Q9UQQ2 Q59H48 LinkDB All DBs Position 12:111404730..111451623 Genome browser AA seq 575 aa AA seqDB search MNGPALQPSSPSSAPSASPAAAPRGWSEFCELHAVAAARELARQYWLFAREHPQHAPLRA ELVSLQFTDLFQRYFCREVRDGRAPGRDYRDTGRGPPAKAEASPEPGPGPAAPGLPKARS SEELAPPRPPGPCSFQHFRRSLRHIFRRRSAGELPAAHTAAAPGTPGEAAETPARPGLAK KFLPWSLAREPPPEALKEAVLRYSLADEASMDSGARWQRGRLALRRAPGPDGPDRVLELF DPPKSSRPKLQAACSSIQEVRWCTRLEMPDNLYTFVLKVKDRTDIIFEVGDEQQLNSWMA ELSECTGRGLESTEAEMHIPSALEPSTSSSPRGSTDSLNQGASPGGLLDPACQKTDHFLS CYPWFHGPISRVKAAQLVQLQGPDAHGVFLVRQSETRRGEYVLTFNFQGIAKHLRLSLTE RGQCRVQHLHFPSVVDMLHHFQRSPIPLECGAACDVRLSSYVVVVSQPPGSCNTVLFPFS LPHWDSESLPHWGSELGLPHLSSSGCPRGLSPEGLPGRSSPPEQIFHLVPSPEELANSLQ HLEHEPVNRARDSDYEMDSSSRSHLRAIDNQYTPL NT seq 1728 nt NT seq  +upstreamnt  +downstreamnt atgaacgggcctgccctgcagccctcctcgccctcttccgcgccctcagcctccccggcg gcggccccgcggggctggagcgagttctgtgagttgcacgccgtagcggcggcccgggag ctggcccgccagtactggctgttcgcccgggagcatccgcagcacgcgccgctgcgcgcc gagctggtgtcgctgcagttcaccgacctcttccagcgctacttctgccgcgaggtgcgc gacggacgggcgccgggccgcgactaccgggacacaggccgtgggcccccagccaaggcc gaggcgtccccggagccaggccccggccccgccgcccctggcctgcccaaggcccgcagc tctgaggagctggccccgccgcggccgcccgggccctgctccttccagcactttcgccgc agcctccgccacatcttccgccgccgctcggccggggagctgccagcggcccacaccgct gccgcccccgggacccccggagaggctgctgagacccccgcccggcctggcctggccaag aagttcctgccctggagcctggcccgggagccgccacccgaggcgctgaaggaggcggtg ctgcgctacagcctggccgacgaggcctccatggacagcggggcacgctggcagcgcggg aggctggcgctgcgccgggccccgggccccgatggccccgaccgcgtgctggagctcttc gacccacccaagagttcaaggcccaagctacaagcagcttgctccagcatccaggaggtc cggtggtgcacacggcttgagatgcctgacaacctttacacctttgtgctgaaggtgaag gaccggacagacatcatctttgaggtgggagacgagcagcagctgaattcatggatggct gagctctcggagtgcacaggccgagggctggagagcacagaagcagagatgcatattccc tcagccctagagcctagcacgtccagctccccaaggggcagcacagattcccttaaccaa ggtgcttctcctggggggctgctggacccggcctgccagaagacggaccatttcctgtcc tgctacccctggttccacggccccatctccagagtgaaagcagctcagctggttcagctg cagggccctgatgctcatggagtgttcctggtgcggcagagcgagacgcggcgtggggaa tacgtgctcactttcaactttcaggggatagccaagcacctgcgcctgtcgctgacagag cggggccagtgccgtgtgcagcacctccactttccctcggtcgtggacatgctccaccac ttccagcgctcgcccatcccactcgagtgcggcgccgcctgtgatgtccggctctccagc tacgtggtagtcgtctcccaaccaccaggttcctgcaacacggtcctcttccctttctcc cttcctcactgggattcagagtcccttcctcactggggttcagagttgggccttccccac cttagttcttctggctgtccccgggggctcagcccagagggtctcccagggcgatcctca ccccccgagcagatcttccacctggtgccttcgcccgaagaactggccaacagcctgcag cacctggagcatgagcctgtgaatcgagcccgggactcggactacgaaatggactcatcc tcccggagccacctgcgggccatagacaatcagtacacacctctctga

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