GPSM3
G-protein-signaling modulator 3
Also known as: AGS4, C6orf9, G18, G18.1a, G18.1b, G18.2, GPSM3_HUMAN, NG1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y4H4
- Gene
- GPSM3
- Ensembl
- ENSG00000213654
- Chromosome
- 6
- Canonical length
- 160 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable GTPase regulator activity. Predicted to be involved in positive regulation of inflammatory response. Predicted to act upstream of or within positive regulation of cytokine production involved in inflammatory response and positive regulation of leukocyte chemotaxis. Predicted to be located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
160 residues, UniProt reviewed canonical sequence.
>Q9Y4H4|GPSM3
1 MEAERPQEEE DGEQGPPQDE EGWPPPNSTT RPWRSAPPSP PPPGTRHTAL GPRSASLLSL
61 QTELLLDLVA EAQSRRLEEQ RATFYTPQNP SSLAPAPLRP LEDREQLYST ILSHQCQRME
121 AQRSEPPLPP GGQELLELLL RVQGGGRMEE QRSRPPTHTCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPSM3 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)
- 0.61
- Highest tissue expression
- 235 nTPM
Expression across tissuesHPA
Tissue
- spleen: 235 nTPM
- bone marrow: 152 nTPM
- lymph node: 131 nTPM
- tonsil: 94 nTPM
- appendix: 91 nTPM
- thymus: 77 nTPM
Single-cell type
- microglia: 32 nCPM
- megakaryocytes: 19 nCPM
- neutrophils: 17 nCPM
- platelets: 14 nCPM
- b-cells: 8.9 nCPM
- nk-cells: 8.1 nCPM
Immune cell
- neutrophil: 246 nTPM
- eosinophil: 195 nTPM
- intermediate monocyte: 73 nTPM
- non-classical monocyte: 72 nTPM
- myeloid DC: 58 nTPM
- classical monocyte: 56 nTPM
Brain region
- medulla oblongata: 17 nTPM
- thalamus: 15 nTPM
- white matter: 14 nTPM
- pons: 13 nTPM
- hypothalamus: 13 nTPM
- midbrain: 12 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)
- 0.79
- gnomAD pLI
- 0.29
- gnomAD missense Z
- 0.87
- DepMap mean gene effect
- -0.17
- 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
- positive regulation of cytokine production involved in inflammatory response
- positive regulation of inflammatory response
- positive regulation of leukocyte chemotaxis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- GoLoco motif
- Tetratricopeptide-like helical domain superfamily
- GoLoco motif
- G-protein-signaling modulator 3
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPSM3 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 GPSM3 as an antibody target. Whether an autoantibody or antibody against GPSM3 could matter depends on whether native GPSM3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPSM3 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 GPSM3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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