SCUBA

ARAP1 — ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1

ARAP1 belongs to a gene co-expression module in 1 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.

ARAP1's module in each cell type

Cell typeModuleShares the module with
MacrophagesSplicing Factor Regulation
Housekeeping
CCNL1, CELF1, CLK1, FAM53C, IFRD1, INPPL1, KIDINS220, MAN2C1 +12 moreView in SCUBA

About the gene

SynonymsCENTD2
Chromosome11: 72685069-72793599
Predicted locationIntracellular
Essential geneNo
Protein classPredicted intracellular proteins
Molecular functionGTPase activation

Function

Phosphatidylinositol 3,4,5-trisphosphate-dependent GTPase- activating protein that modulates actin cytoskeleton remodeling by regulating ARF and RHO family members. Activated by phosphatidylinositol 3,4,5-trisphosphate (PtdIns(3,4,5)P3) binding and, to a lesser extent, by phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P2) binding. Has a preference for ARF1 and ARF5. Positively regulates the ring size of circular dorsal ruffles and promotes macropinocytosis. Acts as a bridging factor in osteoclasts to control actin and membrane dynamics (By similarity). Regulates the condensing of osteoclast podosomes into sealing zones which segregate the bone-facing membrane from other membrane domains and are required for osteoclast resorption activity (By similarity). Also regulates recruitment of the AP-3 complex to endosomal membranes and trafficking of lysosomal membrane proteins to the ruffled membrane border of osteoclasts to modulate bone resorption (By similarity). Regulates the endocytic trafficking of EGFR. Regulates the incorporation of CD63 and CD9 into multivesicular bodies. Required in the retinal pigment epithelium (RPE) for photoreceptor survival due to its role in promoting RPE phagocytosis (By similarity).

Human Protein Atlas · Open Targets · UniProt

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