Homo sapiens (human): 3937 Help Entry 3937              CDS       T01001                                  Symbol LCP2, IMD81, SLP-76, SLP76 Name (RefSeq) lymphocyte cytosolic protein 2   KO K07361   lymphocyte cytosolic protein 2 Organism hsa  Homo sapiens (human) Pathway hsa04015   Rap1 signaling pathway hsa04380   Osteoclast differentiation hsa04611   Platelet activation hsa04650   Natural killer cell mediated cytotoxicity hsa04660   T cell receptor signaling pathway hsa04664   Fc epsilon RI signaling pathway hsa05135   Yersinia infection Network nt06183  Yersinia nt06537  TCR/BCR signaling   Element N01106   TCR-PLCG-ITPR signaling pathway N01108   Yersinia YopH to TCR-NFAT signaling pathway Disease H02526   Disorders of adaptive immunity Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04015 Rap1 signaling pathway     3937 (LCP2)  09150 Organismal Systems   09151 Immune system    04611 Platelet activation     3937 (LCP2)    04650 Natural killer cell mediated cytotoxicity     3937 (LCP2)    04660 T cell receptor signaling pathway     3937 (LCP2)    04664 Fc epsilon RI signaling pathway     3937 (LCP2)   09158 Development and regeneration    04380 Osteoclast differentiation     3937 (LCP2)  09160 Human Diseases   09171 Infectious disease: bacterial    05135 Yersinia infection     3937 (LCP2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SH2 SAM_2 SAM_1 DUF7145 Motif Other DBs NCBI-GeneID:  3937 NCBI-ProteinID:  NP_005556 OMIM:  601603 HGNC:  6529 Ensembl:  ENSG00000043462 UniProt:  Q13094 Structure PDBPDBj LinkDB All DBs Position 5:complement(170246233..170297777) Genome browser AA seq 533 aa AA seqDB search MALRNVPFRSEVLGWDPDSLADYFKKLNYKDCEKAVKKYHIDGARFLNLTENDIQKFPKL RVPILSKLSQEINKNEERRSIFTRKPQVPRFPEETESHEEDNGGWSSFEEDDYESPNDDQ DGEDDGDYESPNEEEEAPVEDDADYEPPPSNDEEALQNSILPAKPFPNSNSMYIDRPPSG KTPQQPPVPPQRPMAALPPPPAGRNHSPLPPPQTNHEEPSRSRNHKTAKLPAPSIDRSTK PPLDRSLAPFDREPFTLGKKPPFSDKPSIPAGRSLGEHLPKIQKPPLPPTTERHERSSPL PGKKPPVPKHGWGPDRRENDEDDVHQRPLPQPALLPMSSNTFPSRSTKPSPMNPLPSSHM PGAFSESNSSFPQSASLPPYFSQGPSNRPPIRAEGRNFPLPLPNKPRPPSPAEEENSLNE EWYVSYITRPEAEAALRKINQDGTFLVRDSSKKTTTNPYVLMVLYKDKVYNIQIRYQKES QVYLLGTGLRGKEDFLSVSDIIDYFRKMPLLLIDGKNRGSRYQCTLTHAAGYP NT seq 1602 nt NT seq  +upstreamnt  +downstreamnt atggcactgaggaatgtgccctttcgctcagaggtcctgggctgggaccccgacagcctt gctgactatttcaagaagctcaactataaggactgtgagaaggcagtgaagaagtaccac atcgatggggctcgcttcttgaacctgacagaaaatgacatccagaagttccccaagctc cgggtgccgattctcagtaagttaagtcaggaaatcaacaagaacgaagagaggaggagc atcttcacacgcaaaccccaagtcccgcggtttcctgaagagacagaaagccacgaagag gacaatgggggctggtcgtcctttgaagaagacgattatgaaagtcccaatgatgaccag gatggggaggatgatggagactatgagtcccccaatgaggaggaagaggcacccgtggaa gatgacgcggattatgagccgccaccctccaatgacgaggaagctctgcagaactccatc ctgcctgccaagcctttccccaactccaactccatgtacatcgaccggcccccctctggg aaaaccccccagcagcctcctgtgcccccccagagaccgatggccgccctcccgccccca ccagccggccggaatcactcgccactgcccccaccccagaccaaccacgaagaacccagc agaagcagaaaccacaaaacggcaaagctccctgctccttcaatagacagaagcacgaaa cctcccctagatcgttcattagctccgtttgatagagaacccttcacactaggaaagaaa ccaccattttctgacaagccctcgattccagcgggaaggtcactcggggagcatttaccc aagattcaaaagcctcctttaccaccgaccacggaaagacatgaaaggagcagccccctg ccagggaagaagccacctgtgccaaagcatggatggggaccagacagaagagagaatgat gaagatgatgtgcatcagagacctttgccccagccagcactacttcctatgagctccaac actttcccttcaagatctactaagccaagtcccatgaaccctctcccatcctctcacatg cctggagcattctcagaaagtaacagcagttttccacagagtgcctccctgccaccatac ttctctcaaggccctagcaacagaccacctatcagagccgaaggcagaaacttccccttg ccacttccaaacaaacctcggcccccatcccccgcggaggaagagaattcattaaatgaa gagtggtacgtttcttatattacccgaccagaggcagaagctgctcttagaaagataaac caggatggcacatttctggtcagagacagctctaaaaaaacaacaaccaatccatatgtc ctcatggtgttgtacaaagataaagtttacaacatccagatccgttatcagaaggaaagt caagtttacttgttgggaactggactccgagggaaagaggactttctgtctgtgtcagat attattgactacttcaggaaaatgccacttctgctcattgatgggaaaaaccgaggttcc agataccagtgcacattaacgcatgctgcagggtacccatag

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