SCUBA

ARID4A — AT-rich interaction domain 4A

ARID4A belongs to a gene co-expression module in 2 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

ARID4A's module in each cell type

Cell typeModuleShares the module with
Innate lymphoid cellsCentrosome & Scaffolding
Cytoskeleton & motility
AKAP9, APPL1, CCDC91, CPNE3, ETNK1, FAM204A, GOPC, LRBA +14 moreView in SCUBA
MacrophagesChromatin Regulatory Genes
Housekeeping
ACAP2, ATRX, BPTF, BRD10, BRD4, EP300, ERBIN, ETNK1 +31 moreView in SCUBA

About the gene

SynonymsRBBP1, RBP-1, RBP1
Chromosome14: 58298504-58373887
Predicted locationIntracellular
Essential geneNo
Protein classPredicted intracellular proteins, Transcription factors
Molecular functionChromatin regulator, DNA-binding
Biological processDifferentiation, Spermatogenesis, Transcription, Transcription regulation

Function

DNA-binding protein which modulates activity of several transcription factors including RB1 (retinoblastoma-associated protein) and AR (androgen receptor) (By similarity). May function as part of an mSin3A repressor complex. Has no intrinsic transcriptional activity (By similarity). Plays a role in the regulation of epigenetic modifications at the PWS/AS imprinting center near the SNRPN promoter, where it might function as part of a complex with RB1 and ARID4B (By similarity). Involved in spermatogenesis, together with ARID4B, where it acts as a transcriptional coactivator for AR and enhances expression of genes required for sperm maturation. Regulates expression of the tight junction protein CLDN3 in the testis, which is important for integrity of the blood-testis barrier (By similarity). Plays a role in myeloid homeostasis where it regulates the histone methylation state of bone marrow cells and expression of various genes involved in hematopoiesis. May function as a leukemia suppressor (By similarity).

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.