ARHGAP39
Rho GTPase-activating protein 39
Also known as: CrGAP, KIAA1688, RHG39_HUMAN, Vilse
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9C0H5
- Gene
- ARHGAP39
- Ensembl
- ENSG00000147799
- Chromosome
- 8
- Canonical length
- 1083 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable GTPase activator activity. Involved in postsynapse organization. Is active in glutamatergic synapse. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1083 residues, UniProt reviewed canonical sequence.
>Q9C0H5|ARHGAP39
1 MSQTQDYECR SHNVDLPESR IPGSNTRLEW VEIIEPRTRE RMYANLVTGE CVWDPPAGVR
61 IKRTSENQWW ELFDPNTSRF YYYNASTQRT VWHRPQGCDI IPLAKLQTLK QNTESPRASA
121 ESSPGRGSSV SREGSTSSSL EPEPDTEKAQ ELPARAGRPA AFGTVKEDSG SSSPPGVFLE
181 KDYEIYRDYS ADGQLLHYRT SSLRWNSGAK ERMLIKVADR EPSFLAAQGN GYAPDGPPGV
241 RSRRPSGSQH SPSLQTFAPE ADGTIFFPER RPSPFLKRAE LPGSSSPLLA QPRKPSGDSQ
301 PSSPRYGYEP PLYEEPPVEY QAPIYDEPPM DVQFEAGGGY QAGSPQRSPG RKPRPFLQPN
361 KQGPPSPCQQ LVLTKQKCPE RFLSLEYSPA GKEYVRQLVY VEQAGSSPKL RAGPRHKYAP
421 NPGGGSYSLQ PSPCLLRDQR LGVKSGDYST MEGPELRHSQ PPTPLPQAQE DAMSWSSQQD
481 TLSSTGYSPG TRKRKSRKPS LCQATSATPT EGPGDLLVEQ PLAEEQPPCG TSLAPVKRAE
541 GEAEGARGAA EPFLAQARLA WEAQQAHFHM KQRSSWDSQQ DGSGYESDGA LPLPMPGPVV
601 RAFSEDEALA QQENRHWRRG TFEKLGFPQI LLEKSVSVQT NLASPEPYLH PSQSEDLAAC
661 AQFESSRQSR SGVPSSSCVF PTFTLRKPSS ETDIENWASK HFNKHTQGLF RRKVSIANML
721 AWSSESIKKP MIVTSDRHVK KEACELFKLI QMYMGDRRAK ADPLHVALEV ATKGWSVQGL
781 RDELYIQLCR QTTENFRLES LARGWELMAI CLAFFPPTPK FHSYLEGYIY RHMDPVNDTK
841 GVAISTYAKY CYHKLQKAAL TGAKKGLKKP NVEEIRHAKN AVFSPSMFGS ALQEVMGMQR
901 ERYPERQLPW VQTRLSEEVL ALNGDQTEGI FRVPGDIDEV NALKLQVDQW KVPTGLEDPH
961 VPASLLKLWY RELEEPLIPH EFYEQCIAHY DSPEAAVAVV HALPRINRMV LCYLIRFLQV
1021 FVQPANVAVT KMDVSNLAMV MAPNCLRCQS DDPRVIFENT RKEMSFLRVL IQHLDTSFME
1081 GVLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ARHGAP39 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)
- 0.5
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- testis: 20 nTPM
- spinal cord: 16 nTPM
- cerebral cortex: 15 nTPM
- cerebellum: 14 nTPM
- hippocampal formation: 12 nTPM
- hypothalamus: 9.6 nTPM
Single-cell type
- respiratory ciliated cells: 135 nCPM
- endometrial ciliated cells: 131 nCPM
- ependymal cells: 107 nCPM
- fallopian tube ciliated cells: 86 nCPM
- schwann cells: 82 nCPM
- epididymal efferent duct ciliated cells: 75 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
- cerebral cortex: 38 nTPM
- white matter: 38 nTPM
- medulla oblongata: 37 nTPM
- hippocampal formation: 37 nTPM
- midbrain: 32 nTPM
- pons: 29 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)
- 0.45
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 2.52
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ARHGAP39 as an antibody target. Whether an autoantibody or antibody against ARHGAP39 could matter depends on whether native ARHGAP39 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ARHGAP39 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 ARHGAP39 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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