ARHGAP28
Rho GTPase-activating protein 28
Also known as: FLJ10312, KIAA1314, RHG28_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P2N2
- Gene
- ARHGAP28
- Ensembl
- ENSG00000088756
- Chromosome
- 18
- Canonical length
- 729 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cell Junctions
OverviewNCBI Gene
Predicted to enable GTPase activator activity. Predicted to be involved in negative regulation of stress fiber assembly; regulation of actin filament polymerization; and regulation of small GTPase mediated signal transduction. Located in cell junction and nucleoplasm. Implicated in allergic disease. Biomarker of meningioma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
729 residues, UniProt reviewed canonical sequence.
>Q9P2N2|ARHGAP28
1 MEVEDSGGVV LTAYHSYARA QPPNAESRCA PRAAASHPLS RKSIPRCRRI NRMLSNESLH
61 PPAFSRSNSE ASVDSASMED FWREIESIKD SSMGGQEEPP PAEVTPVDEG ELEAEWLQDV
121 GLSTLISGDE EEDGKALLST LTRTQAAAVQ KRYHTYTQTM RKKDKQSIRD VRDIFGVSES
181 PPRDTCGNHT NQLDGTKEER ELPRVIKTSG SMPDDASLNS TTLSDASQDK EGSFAVPRSD
241 SVAILETIPV LPVHSNGSPE PGQPVQNAIS DDDFLEKNIP PEAEELSFEV SYSEMVTEAL
301 KRNKLKKSEI KKEDYVLTKF NVQKTRFGLT EAGDLSAEDM KKIRHLSLIE LTAFFDAFGI
361 QLKRNKTEKV KGRDNGIFGV PLTVLLDGDR KKDPGVKVPL VLQKFFEKVE ESGLESEGIF
421 RLSGCTAKVK QYREELDAKF NADKFKWDKM CHREAAVMLK AFFRELPTSL FPVEYIPAFI
481 SLMERGPHVK VQFQALHLMV MALPDANRDA AQALMTFFNK VIANESKNRM SLWNISTVMA
541 PNLFFSRSKH SDYEELLLAN TAAHIIRLML KYQKILWKVP SFLITQVRRM NEATMLLKKQ
601 LPSVRKLLRR KTLERETASP KTSKVLQKSP SARRMSDVPE GVIRVHAPLL SKVSMAIQLN
661 NQTKAKDILA KFQYENSHGS SECIKIQNQR LYEIGGNIGE HCLDPDAYIL DVYRINPQAE
721 WVIKPQQSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGAP28 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)
- 0.41
- Highest tissue expression
- 72 nTPM
Expression across tissuesHPA
Tissue
- testis: 72 nTPM
- placenta: 24 nTPM
- spleen: 12 nTPM
- epididymis: 8.2 nTPM
- cervix: 8.1 nTPM
- kidney: 7.9 nTPM
Single-cell type
- podocytes: 1,006 nCPM
- late spermatids: 704 nCPM
- early spermatids: 623 nCPM
- late primary spermatocytes: 255 nCPM
- mesothelial cells: 234 nCPM
- prostatic glandular cells: 139 nCPM
Immune cell
- neutrophil: 2.9 nTPM
- basophil: 0.6 nTPM
- eosinophil: 0.3 nTPM
- classical monocyte: 0.2 nTPM
- naive B-cell: 0.2 nTPM
- plasmacytoid DC: 0.2 nTPM
Brain region
- cerebellum: 11 nTPM
- hypothalamus: 11 nTPM
- cerebral cortex: 11 nTPM
- basal ganglia: 10 nTPM
- hippocampal formation: 10 nTPM
- amygdala: 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)
- 0.86
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of stress fiber assembly
- regulation of actin filament polymerization
- regulation of small GTPase mediated signal transduction
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ARHGAP28 as an antibody target. Whether an autoantibody or antibody against ARHGAP28 could matter depends on whether native ARHGAP28 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGAP28 is annotated at the cell surface, where native ARHGAP28 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 ARHGAP28 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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