Homo sapiens (human): 5993 Help Entry 5993              CDS       T01001                                  Gene name RFX5 Definition (RefSeq) regulatory factor X5   KO K08061   regulatory factor X 5 Organism hsa  Homo sapiens (human) Pathway hsa04612   Antigen processing and presentation hsa05152   Tuberculosis hsa05340   Primary immunodeficiency Disease H00093   Combined immunodeficiency H00985   Bare lymphocyte syndrome type2 Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09151 Immune system    04612 Antigen processing and presentation     5993 (RFX5)  09160 Human Diseases   09163 Immune disease    05340 Primary immunodeficiency     5993 (RFX5)   09171 Infectious disease: bacterial    05152 Tuberculosis     5993 (RFX5)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     5993 (RFX5) Transcription factors [BR:hsa03000]  Eukaryotic type   Other basic domains    RF-X     5993 (RFX5) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  RFX5_DNA_bdg RFX5_N RFX_DNA_binding Pox_D5 Motif Other DBs NCBI-GeneID:  5993 NCBI-ProteinID:  NP_000440 OMIM:  601863 HGNC:  9986 Ensembl:  ENSG00000143390 Vega:  OTTHUMG00000012495 Pharos:  P48382(Tbio) UniProt:  P48382 LinkDB All DBs Structure PDB:  2KW3 Thumbnails Position 1q21.3 AA seq 616 aa AA seqDB search MAEDEPDAKSPKTGGRAPPGGAEAGEPTTLLQRLRGTISKAVQNKVEGILQDVQKFSDND KLYLYLQLPSGPTTGDKSSEPSTLSNEEYMYAYRWIRNHLEEHTDTCLPKQSVYDAYRKY CESLACCRPLSTANFGKIIREIFPDIKARRLGGRGQSKYCYSGIRRKTLVSMPPLPGLDL KGSESPEMGPEVTPAPRDELVEAACALTCDWAERILKRSFSSIVEVARFLLQQHLISARS AHAHVLKAMGLAEEDEHAPRERSSKPKNGLENPEGGAHKKPERLAQPPKDLEARTGAGPL ARGERKKSVVESSAPGANNLQVNALVARLPLLLPRAPRSLIPPIPVSPPILAPRLSSGAL KVATLPLSSRAGAPPAAVPIINMILPTVPALPGPGPGPGRAPPGGLTQPRGTENREVGIG GDQGPHDKGVKRTAEVPVSEASGQAPPAKAAKQDIEDTASDAKRKRGRPRKKSGGSGERN STPLKSAAAMESAQSSRLPWETWGSGGEGNSAGGAERPGPMGEAEKGAVLAQGQGDGTVS KGGRGPGSQHTKEAEDKIPLVPSKVSVIKGSRSQKEAFPLAKGEVDTAPQGNKDLKEHVL QSSLSQEHKDPKATPP NT seq 1851 nt NT seq  +upstreamnt  +downstreamnt atggcagaagatgagcctgatgctaagagccccaagactgggggaagggcccccccaggt ggtgctgaggctggggaacctaccacccttcttcagaggctccgaggtaccatttccaag gccgtgcagaacaaagtagaggggatcctgcaagatgtacagaaattttctgacaatgac aagctgtatctctaccttcagctcccctcaggacccaccactggagacaaaagctcagag ccaagtacactgagcaatgaggagtacatgtatgcctataggtggatccgcaaccacctg gaagagcacactgacacctgtctgccaaagcaaagtgtttatgatgcctatcggaagtac tgtgagagtcttgcctgttgccgcccactcagcacagccaactttggcaagatcatcaga gagatcttccctgacatcaaagctcgaaggcttggtggccggggccagtccaaatattgc tacagtggcataaggaggaagaccttggtgtctatgccacccctgcctggacttgaccta aagggttctgagagtccagaaatgggcccagaagtaaccccagcacctcgagatgaactg gtggaggcagcgtgtgccctgacctgtgactgggcagagcggatcctgaaacggtccttc agttccatcgttgaggtcgcccgcttcctgctacagcagcatctcatctctgcccgatct gcacatgcccatgtgcttaaggccatggggctcgctgaagaggacgaacatgcacctcgg gaacggtcatctaaaccaaagaatggtttagagaacccagagggtggagcccacaagaag ccagagagactggcccagcctcctaaggatctggaagcccgaactggggccggtcctctc gcacgtggagagcggaagaagagtgtagttgagagctcggccccaggagccaataacctg caggttaatgccctagtggctcggctgcctctgctccttccccgggcccctcgctcacta attccgccaatcccagtctctccacctattctggcccccaggctttcttcaggtgccctg aaagtggctacactgcctctgtctagtagggccggggcacccccagcagctgtgcccatc attaacatgatcttaccaactgttcctgctttgcctggacctggacctgggcctgggcga gctccacctgggggactcactcagccccggggcacagagaacagagaggtaggcataggt ggtgaccaaggaccacatgacaagggtgtcaagaggacagctgaagtacctgtgagtgag gccagtgggcaggctccaccagctaaagcagcaaagcaggatatagaggatacagcaagt gatgccaaaaggaaacgggggcgccctcgaaaaaagtcaggtggaagtggggaaaggaat tctacccctctcaagtcagcagctgccatggaatctgcccagtcctcaaggttaccatgg gagacatggggctcaggaggggaaggcaactcagctggaggggcagagaggccagggcca atgggagaggctgaaaagggggcagtacttgcccagggtcagggagatggtactgtttcc aaaggaggaaggggccccggttcccagcataccaaagaagcagaagataaaattcccttg gtcccctcaaaagtgagtgtcatcaagggcagcagaagccaaaaggaggcttttcctttg gcaaagggagaggtagacactgcaccacagggtaataaagacttaaaggagcatgtgctt caaagttccttatcccaggagcataaagacccaaaagcaacacccccatga

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