RFXAP

Description		regulatory factor X associated protein
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GO Annotations	Cellular Component	Nucleus Nuclear Speck
	Molecular Function	DNA Binding DNA-binding Transcription Factor Activity Transcription Coactivator Activity
	Biological Process	Positive Regulation Of Transcription, DNA-templated
Pathways
Drugs
Diseases		Bare lymphocyte syndrome (BLS) type2 Combined immunodeficiencies (CIDs), including the following nine diseases: X-linked hyper IgM syndrome; CD40 deficiency hyper IgM syndrome; Purine nucleoside phosphorylase (PNP) deficiency; Omenn syndrome; MHC deficiency (HLA-class I); MHC deficiency (HLA-class II); Zap-70 deficiency; p56 Lck deficiency; CD8 deficiency
GWAS		Metabolite levels ( 23823483) Perioperative myocardial infarction in coronary artery bypass surgery ( 25948407)
Interacting Genes		4 interacting genes: EPS8 RFX5 RFXANK SMARCA4
Entrez ID		5994
HPRD ID		03515
Ensembl ID		ENSG00000133111
Uniprot IDs		O00287
PDB IDs		2KW3
Enriched GO Terms of Interacting Partners?
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