SCUBA

ARHGAP26 — Rho GTPase activating protein 26

ARHGAP26 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.

ARHGAP26's module in each cell type

Cell typeModuleShares the module with
EndothelialIL33 Alarmin Signaling
Inflammation
CHN1, DOC2B, IL33, MCUB, PTAFR, SDCBP, SLC8A1, STMN3 +1 moreView in SCUBA
EnterocytesYAP cytoskeletal remodeling
Migration & adhesion
ABLIM1, AHCYL2, CCSER1, CDC42BPA, FGD4, ITGB8, PDE4D, PIP5K1B +5 moreView in SCUBA
Gamma-delta T cellsTCR-Cytokine Signaling
TCR Signaling
CACNA2D2, CCDC88C, LPGAT1, LY75, MED15, NBPF14, NBPF19, NBPF20 +10 more
MacrophagesMAPK Stress Kinase
Inflammatory
BRAF, BTBD9, CRY1, CYTH3, EIF2AK3, ESYT2, EXT1, FOXK2 +12 moreView in SCUBA
Mucosal-associated invariant T cellImmune Synapse Signaling
TCR Signaling
APC, ASXL2, CD46, CPSF2, DOCK8, EEA1, EIF4G3, EPB41 +21 more

About the gene

SynonymsGRAF, KIAA0621, OPHN1L, OPHN1L1
Chromosome5: 142770377-143229011
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classCancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins
Molecular functionGTPase activation

Function

GTPase-activating protein for RHOA and CDC42. Facilitates mitochondrial quality control by promoting Parkin-mediated recruitment of autophagosomes to damaged mitochondria. Negatively regulates the growth of human parainfluenza virus type 2 by inhibiting hPIV-2-mediated RHOA activation via interaction with two of its viral proteins P and V. Associates with MICAL1 on the endosomal membrane to promote Rab8-Rab10-dependent tubule extension. After dissociation of MICAL1, recruits WDR44 which connects the endoplasmic reticulum (ER) with the endosomal tubule, thereby participating in the export of a subset of neosynthesized proteins

Human Protein Atlas · Open Targets · UniProt

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