ARHGAP9
Rho GTPase-activating protein 9
Also known as: 10C, MGC1295, RHG09_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BRR9
- Gene
- ARHGAP9
- Ensembl
- ENSG00000123329
- Chromosome
- 12
- Canonical length
- 750 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cell Junctions
OverviewNCBI Gene
This gene encodes a member of the Rho-GAP family of GTPase activating proteins. The protein has substantial GAP activity towards several Rho-family GTPases in vitro, converting them to an inactive GDP-bound state. It is implicated in regulating adhesion of hematopoietic cells to the extracellular matrix. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
750 residues, UniProt reviewed canonical sequence.
>Q9BRR9|ARHGAP9
1 MLSSRWWPSS WGILGLGPRS PPRGSQLCAL YAFTYTGADG QQVSLAEGDR FLLLRKTNSD
61 WWLARRLEAP STSRPIFVPA AYMIEESIPS QSPTTVIPGQ LLWTPGPKLF HGSLEELSQA
121 LPSRAQASSE QPPPLPRKMC RSVSTDNLSP SLLKPFQEGP SGRSLSQEDL PSEASASTAG
181 PQPLMSEPPV YCNLVDLRRC PRSPPPGPAC PLLQRLDAWE QHLDPNSGRC FYINSLTGCK
241 SWKPPRRSRS ETNPGSMEGT QTLKRNNDVL QPQAKGFRSD TGTPEPLDPQ GSLSLSQRTS
301 QLDPPALQAP RPLPQLLDDP HEVEKSGLLN MTKIAQGGRK LRKNWGPSWV VLTGNSLVFY
361 REPPPTAPSS GWGPAGSRPE SSVDLRGAAL AHGRHLSSRR NVLHIRTIPG HEFLLQSDHE
421 TELRAWHRAL RTVIERLVRW VEARREAPTG RDQGSGDREN PLELRLSGSG PAELSAGEDE
481 EEESELVSKP LLRLSSRRSS IRGPEGTEQN RVRNKLKRLI AKRPPLQSLQ ERGLLRDQVF
541 GCQLESLCQR EGDTVPSFLR LCIAAVDKRG LDVDGIYRVS GNLAVVQKLR FLVDRERAVT
601 SDGRYVFPEQ PGQEGRLDLD STEWDDIHVV TGALKLFLRE LPQPLVPPLL LPHFRAALAL
661 SESEQCLSQI QELIGSMPKP NHDTLRYLLE HLCRVIAHSD KNRMTPHNLG IVFGPTLFRP
721 EQETSDPAAH ALYPGQLVQL MLTNFTSLFPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGAP9 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)
- 0.46
- Highest tissue expression
- 113 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 113 nTPM
- spleen: 97 nTPM
- tonsil: 57 nTPM
- lymph node: 53 nTPM
- small intestine: 35 nTPM
- thymus: 33 nTPM
Single-cell type
- neutrophils: 429 nCPM
- late primary spermatocytes: 204 nCPM
- nk-cells: 147 nCPM
- neutrophil progenitors: 142 nCPM
- pdcs: 107 nCPM
- innate lymphoid cells: 79 nCPM
Immune cell
- neutrophil: 393 nTPM
- eosinophil: 245 nTPM
- plasmacytoid DC: 98 nTPM
- intermediate monocyte: 90 nTPM
- classical monocyte: 87 nTPM
- myeloid DC: 72 nTPM
Brain region
- pons: 15 nTPM
- cerebral cortex: 14 nTPM
- cerebellum: 14 nTPM
- medulla oblongata: 11 nTPM
- white matter: 11 nTPM
- thalamus: 10 nTPM
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)
- 0.84
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.41
- DepMap mean gene effect
- -0.22
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 ARHGAP9 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 ARHGAP9 as an antibody target. Whether an autoantibody or antibody against ARHGAP9 could matter depends on whether native ARHGAP9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGAP9 is annotated at the cell surface, where native ARHGAP9 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 ARHGAP9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...