GPATCH3
G patch domain-containing protein 3
Also known as: FLJ12455, GPATC3, GPTC3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96I76
- Gene
- GPATCH3
- Ensembl
- ENSG00000198746
- Chromosome
- 1
- Canonical length
- 525 aa
- Protein class
- Disease related genes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Predicted to enable nucleic acid binding activity. Involved in negative regulation of RIG-I signaling pathway; negative regulation of type I interferon production; and positive regulation of DNA-templated transcription. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
525 residues, UniProt reviewed canonical sequence.
>Q96I76|GPATCH3
1 MAVPGEAEEE ATVYLVVSGI PSVLRSAHLR SYFSQFREER GGGFLCFHYR HRPERAPPQA
61 APNSALIPTD PAAEGQLLSQ TSATDVRPLS TRDSTPIQTR TCCCVISVRG LAQAQRLIRM
121 YSGRRWLDSH GTWLPGRCLI RRLRLPTEAS GLGSFPFKTR KELQSWKAEN EAFTLADLKQ
181 LPELNPPVLM PRGNVGTPLR VFLELIRACR LPPRIITQLQ LQFPKTGSSR RYGNVPFEYE
241 DSETVEQEEL VYTAEGEEIP QGTYLADIPA SPCGEPEEEV GKEEEEESHS DEDDDRGEEW
301 ERHEALHEDV TGQERTTEQL FEEEIELKWE KGGSGLVFYT DAQFWQEEEG DFDEQTADDW
361 DVDMSVYYDR DGGDKDARDS VQMRLEQRLR DGQEDGSVIE RQVGTFERHT KGIGRKVMER
421 QGWAEGQGLG CRCSGVPEAL DSDGQHPRCK RGLGYHGEKL QPFGQLKRPR RNGLGLISTI
481 YDEPLPQDQT ESLLRRQPPT SMKFRTDMAF VRGSSCASDS PSLPDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPATCH3 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)
- 0.49
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 22 nTPM
- skeletal muscle: 17 nTPM
- skin: 12 nTPM
- liver: 12 nTPM
- tongue: 12 nTPM
- spleen: 11 nTPM
Single-cell type
- syncytiotrophoblasts: 44 nCPM
- differentiating spermatogonia: 31 nCPM
- retinal ganglion cells: 23 nCPM
- undifferentiated spermatogonia: 23 nCPM
- cytotrophoblasts: 21 nCPM
- cone photoreceptor cells: 21 nCPM
Immune cell
- basophil: 30 nTPM
- eosinophil: 22 nTPM
- non-classical monocyte: 19 nTPM
- myeloid DC: 19 nTPM
- classical monocyte: 18 nTPM
- gdT-cell: 16 nTPM
Brain region
- white matter: 19 nTPM
- basal ganglia: 17 nTPM
- cerebral cortex: 16 nTPM
- thalamus: 16 nTPM
- cerebellum: 16 nTPM
- midbrain: 15 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)
- 1.26
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.23
- DepMap mean gene effect
- -0.12
- 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 RIG-I signaling pathway
- negative regulation of type I interferon production
- positive regulation of DNA-templated transcription
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G-patch domain
- G-patch domain
- G patch domain-containing protein 3
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GPATCH3 as an antibody target. Whether an autoantibody or antibody against GPATCH3 could matter depends on whether native GPATCH3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPATCH3 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 GPATCH3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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