Entity Details

Primary name RFXAP
Entity type gene
Source Source Link

Details

PrimaryID5994
RefseqGeneNG_007876
SymbolRFXAP
Nameregulatory factor X associated protein
Chromosome13
Location13q13.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsRFXAP_HUMAN

GO terms

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GOName
GO:0003677 DNA binding
GO:0005634 nucleus
GO:0006357 regulation of transcription by RNA polymerase II
GO:0016607 nuclear speck
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0090575 RNA polymerase II transcription regulator complex

Diseases

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Disease IDSourceNameDescription
209920 OMIMBare lymphocyte syndrome 2 (BLS2)A severe combined immunodeficiency disease with early onset. It is characterized by a profound defect in constitutive and interferon-gamma induced MHC II expression, absence of cellular and humoral T-cell response to antigen challenge, hypogammaglobulinemia and impaired antibody production. The consequence include extreme susceptibility to viral, bacterial and fungal infections. The disease is caused by variants affecting the gene represented in this entry.