ARHGEF25
Rho guanine nucleotide exchange factor 25
Also known as: ARHGP_HUMAN, GEFT, p63RhoGEF
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86VW2
- Gene
- ARHGEF25
- Ensembl
- ENSG00000240771
- Chromosome
- 12
- Canonical length
- 580 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Rho GTPases alternate between an inactive GDP-bound state and an active GTP-bound state, and GEFs facilitate GDP/GTP exchange. This gene encodes a guanine nucleotide exchange factor (GEF) which interacts with Rho GTPases involved in contraction of vascular smooth muscles, regulation of responses to angiotensin II and lens cell differentiation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
Canonical amino-acid sequenceUniProt
580 residues, UniProt reviewed canonical sequence.
>Q86VW2|ARHGEF25
1 MRGGHKGGRC ACPRVIRKVL AKCGCCFARG GRESYSIAGS EGSISASAAS GLAAPSGPSS
61 GLSSGPCSPG PPGPVSGLRR WLDHSKHCLS VETEADSGQA GPYENWMLEP ALATGEELPE
121 LTLLTTLLEG PGDKTQPPEE ETLSQAPESE EEQKKKALER SMYVLSELVE TEKMYVDDLG
181 QIVEGYMATM AAQGVPESLR GRDRIVFGNI QQIYEWHRDY FLQELQRCLK DPDWLAQLFI
241 KHERRLHMYV VYCQNKPKSE HVVSEFGDSY FEELRQQLGH RLQLNDLLIK PVQRIMKYQL
301 LLKDFLKYYN RAGMDTADLE QAVEVMCFVP KRCNDMMTLG RLRGFEGKLT AQGKLLGQDT
361 FWVTEPEAGG LLSSRGRERR VFLFEQIIIF SEALGGGVRG GTQPGYVYKN SIKVSCLGLE
421 GNLQGDPCRF ALTSRGPEGG IQRYVLQAAD PAISQAWIKH VAQILESQRD FLNALQSPIE
481 YQRRESQTNS LGRPRGPGVG SPGRIQLGDQ AQGSTHTPIN GSLPSLLLSP KGEVARALLP
541 LDKQALGDIP QAPHDSPPVS PTPKTPPCQA RLAKLDEDELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGEF25 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.45
- Highest tissue expression
- 144 nTPM
Expression across tissuesHPA
Tissue
- colon: 144 nTPM
- blood vessel: 115 nTPM
- cerebellum: 113 nTPM
- fallopian tube: 102 nTPM
- endometrium: 96 nTPM
- urinary bladder: 91 nTPM
Single-cell type
- vascular smooth muscle cells: 7.8 nCPM
- pericytes: 5.4 nCPM
- smooth muscle cells: 5.1 nCPM
- podocytes: 3.4 nCPM
- endometrial stromal cells: 3.3 nCPM
- fibro-adipogenic progenitors: 3.3 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hippocampal formation: 137 nTPM
- cerebral cortex: 135 nTPM
- white matter: 68 nTPM
- cerebellum: 65 nTPM
- basal ganglia: 59 nTPM
- amygdala: 50 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ARHGEF25.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 104 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.85
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.93
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARHGEF25 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ARHGEF25 as an antibody target. Whether an autoantibody or antibody against ARHGEF25 could matter depends on whether native ARHGEF25 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGEF25 is annotated at the cell surface, where native ARHGEF25 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label ARHGEF25 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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