SCUBA

ASAP1 — ArfGAP with SH3 domain, ankyrin repeat and PH domain 1

ASAP1 belongs to a gene co-expression module in 5 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.

ASAP1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsNFAT activation
TCR/AP1/NFKb pathway
AHI1, BCAT1, BICDL1, CPM, CYP7B1, ETV6, FAM107B, FKBP5 +13 moreView in SCUBA
Lymphatic endothelialRho/Ras GTPase Regulation
Cytoskeletal
CADPS2, CDK17, ERC1, ETV6, KIF13A, LDLRAD4, LMBR1, PLEKHG1 +4 moreView in SCUBA
MacrophagesEndosomal Vesicle Trafficking
Vesicular traficking
ADAM17, AP3B1, ARFGEF1, ARID1B, ARK2N, ATF6, ATP11A, CDC73 +48 moreView in SCUBA
NeutrophilsCytoskeletal Remodeling
Cytoskeletal
ARB2A, ATXN1, GTDC1, HDAC4, MTMR3, NFAT5, ST6GALNAC3, SVIL +2 more
PericytesTGF-β Cytoskeletal Remodeling
Cytoskeletal
ARHGEF12, GRK5, LRRC32, MYH9, RAPGEF2, RFTN1, SERPINH1, TCEAL9 +2 moreView in SCUBA

About the gene

SynonymsCENTB4, DDEF1, KIAA1249, PAP, ZG14P
Chromosome8: 130052104-130443674
Predicted locationIntracellular
Essential geneNo
Protein classPredicted intracellular proteins
Molecular functionGTPase activation
Biological processCilium biogenesis/degradation

Function

Possesses phosphatidylinositol 4,5-bisphosphate-dependent GTPase-activating protein activity for ARF1 (ADP ribosylation factor 1) and ARF5 and a lesser activity towards ARF6. May coordinate membrane trafficking with cell growth or actin cytoskeleton remodeling by binding to both SRC and PIP2. May function as a signal transduction protein involved in the differentiation of fibroblasts into adipocytes and possibly other cell types. Part of the ciliary targeting complex containing Rab11, ASAP1, Rabin8/RAB3IP, RAB11FIP3 and ARF4, which direct preciliary vesicle trafficking to mother centriole and ciliogenesis initiation.

Human Protein Atlas · Open Targets · UniProt

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