Homo sapiens (human): 388 Help Entry 388               CDS       T01001                                  Symbol RHOB, ARH6, ARHB, MST081, MSTP081, RHOH6 Name (RefSeq) ras homolog family member B   KO K07856   Ras homolog gene family, member B Organism hsa  Homo sapiens (human) Pathway hsa05132   Salmonella infection Brite KEGG Orthology (KO) [BR:hsa00001]  09160 Human Diseases   09171 Infectious disease: bacterial    05132 Salmonella infection     388 (RHOB)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04131 Membrane trafficking [BR:hsa04131]     388 (RHOB)   09183 Protein families: signaling and cellular processes    04031 GTP-binding proteins [BR:hsa04031]     388 (RHOB) Membrane trafficking [BR:hsa04131]  Endosome - Lysosome transport   Rab GTPases and associated proteins    Rab associated proteins     388 (RHOB) GTP-binding proteins [BR:hsa04031]  Small (monomeric) G-proteins   Rho Family    RhoA/B/C [OT]     388 (RHOB) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Ras Roc Arf GTP_EFTU Gtr1_RagA SRPRB Motif Other DBs NCBI-GeneID:  388 NCBI-ProteinID:  NP_004031 OMIM:  165370 HGNC:  668 Ensembl:  ENSG00000143878 UniProt:  P62745 Structure PDBPDBj LinkDB All DBs Position 2:20447074..20449440 Genome browser AA seq 196 aa AA seqDB search MAAIRKKLVVVGDGACGKTCLLIVFSKDEFPEVYVPTVFENYVADIEVDGKQVELALWDT AGQEDYDRLRPLSYPDTDVILMCFSVDSPDSLENIPEKWVPEVKHFCPNVPIILVANKKD LRSDEHVRTELARMKQEPVRTDDGRAMAVRIQAYDYLECSAKTKEGVREVFETATRAALQ KRYGSQNGCINCCKVL NT seq 591 nt NT seq  +upstreamnt  +downstreamnt atggcggccatccgcaagaagctggtggtggtgggcgacggcgcgtgtggcaagacgtgc ctgctgatcgtgttcagtaaggacgagttccccgaggtgtacgtgcccaccgtcttcgag aactatgtggccgacattgaggtggacggcaagcaggtggagctggcgctgtgggacacg gcgggccaggaggactacgaccgcctgcggccgctctcctacccggacaccgacgtcatt ctcatgtgcttctcggtggacagcccggactcgctggagaacatccccgagaagtgggtc cccgaggtgaagcacttctgtcccaatgtgcccatcatcctggtggccaacaaaaaagac ctgcgcagcgacgagcatgtccgcacagagctggcccgcatgaagcaggaacccgtgcgc acggatgacggccgcgccatggccgtgcgcatccaagcctacgactacctcgagtgctct gccaagaccaaggaaggcgtgcgcgaggtcttcgagacggccacgcgcgccgcgctgcag aagcgctacggctcccagaacggctgcatcaactgctgcaaggtgctatga

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