ARHGAP19
Rho GTPase-activating protein 19
Also known as: FLJ00194, MGC14258, RHG19_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14CB8
- Gene
- ARHGAP19
- Ensembl
- ENSG00000213390
- Chromosome
- 10
- Canonical length
- 494 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
Members of the ARHGAP family, such as ARHGAP19, encode negative regulators of Rho GTPases (see RHOA; MIM 165390), which are involved in cell migration, proliferation, and differentiation, actin remodeling, and G1 cell cycle progression (Lv et al., 2007 [PubMed 17454002]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
494 residues, UniProt reviewed canonical sequence.
>Q14CB8|ARHGAP19
1 MATEAQSEGE VPARESGRSD AICSFVICND SSLRGQPIIF NPDFFVEKLR HEKPEIFTEL
61 VVSNITRLID LPGTELAQLM GEVDLKLPGG AGPASGFFRS LMSLKRKEKG VIFGSPLTEE
121 GIAQIYQLIE YLHKNLRVEG LFRVPGNSVR QQILRDALNN GTDIDLESGE FHSNDVATLL
181 KMFLGELPEP LLTHKHFNAH LKIADLMQFD DKGNKTNIPD KDRQIEALQL LFLILPPPNR
241 NLLKLLLDLL YQTAKKQDKN KMSAYNLALM FAPHVLWPKN VTANDLQENI TKLNSGMAFM
301 IKHSQKLFKA PAYIRECARL HYLGSRTQAS KDDLDLIASC HTKSFQLAKS QKRNRVDSCP
361 HQEETQHHTE EALRELFQHV HDMPESAKKK QLIRQFNKQS LTQTPGREPS TSQVQKRARS
421 RSFSGLIKRK VLGNQMMSEK KKKNPTPESV AIGELKGTSK ENRNLLFSGS PAVTMTPTRL
481 KWSEGKKEGK KGFLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGAP19 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- thymus: 20 nTPM
- bone marrow: 18 nTPM
- testis: 17 nTPM
- lymph node: 12 nTPM
- tonsil: 12 nTPM
- spleen: 7.4 nTPM
Single-cell type
- oocytes: 4.6 nCPM
- erythrocyte progenitors: 3.6 nCPM
- early spermatids: 3 nCPM
- erythrocytes: 3 nCPM
- late spermatids: 2.8 nCPM
- monocyte progenitors: 2.8 nCPM
Immune cell
- basophil: 22 nTPM
- neutrophil: 16 nTPM
- eosinophil: 11 nTPM
- classical monocyte: 7.2 nTPM
- intermediate monocyte: 6.8 nTPM
- T-reg: 6.4 nTPM
Brain region
- white matter: 15 nTPM
- medulla oblongata: 13 nTPM
- basal ganglia: 12 nTPM
- pons: 10 nTPM
- spinal cord: 10 nTPM
- hypothalamus: 10 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ARHGAP19.
Disease | GeneticClinVar
4 pathogenic / likely-pathogenic of 72 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Charcot-Marie-Tooth disease, axonal, type 2KK
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)
- 1.1
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.34
- DepMap mean gene effect
- -0.05
- 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
- Rho GTPase-activating protein domain
- Rho GTPase activation protein
- RhoGAP domain
- ArhGAP19, RhoGAP domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ARHGAP19 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 ARHGAP19 as an antibody target. Whether an autoantibody or antibody against ARHGAP19 could matter depends on whether native ARHGAP19 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGAP19 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label ARHGAP19 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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