SSTR4
Somatostatin receptor type 4
Also known as: SSR4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P31391
- Gene
- SSTR4
- Ensembl
- ENSG00000132671
- Chromosome
- 20
- Canonical length
- 388 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
Somatostatin acts at many sites to inhibit the release of many hormones and other secretory proteins. The biologic effects of somatostatin are probably mediated by a family of G protein-coupled receptors that are expressed in a tissue-specific manner. SSTR4 is a member of the superfamily of receptors having seven transmembrane segments and is expressed in highest levels in fetal and adult brain and lung. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
388 residues, UniProt reviewed canonical sequence.
>P31391|SSTR4
1 MSAPSTLPPG GEEGLGTAWP SAANASSAPA EAEEAVAGPG DARAAGMVAI QCIYALVCLV
61 GLVGNALVIF VILRYAKMKT ATNIYLLNLA VADELFMLSV PFVASSAALR HWPFGSVLCR
121 AVLSVDGLNM FTSVFCLTVL SVDRYVAVVH PLRAATYRRP SVAKLINLGV WLASLLVTLP
181 IAIFADTRPA RGGQAVACNL QWPHPAWSAV FVVYTFLLGF LLPVLAIGLC YLLIVGKMRA
241 VALRAGWQQR RRSEKKITRL VLMVVVVFVL CWMPFYVVQL LNLFVTSLDA TVNHVSLILS
301 YANSCANPIL YGFLSDNFRR FFQRVLCLRC CLLEGAGGAE EEPLDYYATA LKSKGGAGCM
361 CPPLPCQQEA LQPEPGRKRI PLTRTTTFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SSTR4 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
- 7
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 0.8 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 0.8 nTPM
- cerebral cortex: 0.8 nTPM
- amygdala: 0.7 nTPM
- hippocampal formation: 0.6 nTPM
- basal ganglia: 0.4 nTPM
- fallopian tube: 0.1 nTPM
Single-cell type
- early spermatids: 1.7 nCPM
- late spermatids: 1 nCPM
- late primary spermatocytes: 0.6 nCPM
- adipocytes: 0 nCPM
- adrenal cortex cells: 0 nCPM
- adrenal medulla cells: 0 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
- hippocampal formation: 2.5 nTPM
- cerebral cortex: 2.1 nTPM
- amygdala: 1.6 nTPM
- basal ganglia: 1.6 nTPM
- cerebellum: 1.4 nTPM
- white matter: 0.7 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)
- 1.96
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.23
- DepMap mean gene effect
- 0.05
- 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
- cellular response to glucocorticoid stimulus
- G protein-coupled receptor signaling pathway
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- negative regulation of cell population proliferation
- neuropeptide signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SSTR4 as an antibody target. Whether an autoantibody or antibody against SSTR4 could matter depends on whether native SSTR4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SSTR4 is annotated at the cell surface, where native SSTR4 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 SSTR4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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