GPR174
Probable G-protein coupled receptor 174
Also known as: FKSG79, GP174_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BXC1
- Gene
- GPR174
- Ensembl
- ENSG00000147138
- Chromosome
- X
- Canonical length
- 333 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
- Subcellular location
- Vesicles,Plasma membrane,Centriolar satellite
OverviewNCBI Gene
This gene encodes a protein belonging to the G protein-coupled receptor superfamily. These proteins are characterized by the presence of seven alpha-helical transmembrane domains, and they activate or interact with various endogenous or exogenous ligands, including neurotransmitters, hormones, and odorant and taste substances. This family member is classified as an orphan receptor because the cognate ligand has not been identified. [provided by RefSeq, Sep 2011]
Canonical amino-acid sequenceUniProt
333 residues, UniProt reviewed canonical sequence.
>Q9BXC1|GPR174
1 MPANYTCTRP DGDNTDFRYF IYAVTYTVIL VPGLIGNILA LWVFYGYMKE TKRAVIFMIN
61 LAIADLLQVL SLPLRIFYYL NHDWPFGPGL CMFCFYLKYV NMYASIYFLV CISVRRFWFL
121 MYPFRFHDCK QKYDLYISIA GWLIICLACV LFPLLRTSDD TSGNRTKCFV DLPTRNVNLA
181 QSVVMMTIGE LIGFVTPLLI VLYCTWKTVL SLQDKYPMAQ DLGEKQKALK MILTCAGVFL
241 ICFAPYHFSF PLDFLVKSNE IKSCLARRVI LIFHSVALCL ASLNSCLDPV IYYFSTNEFR
301 RRLSRQDLHD SIQLHAKSFV SNHTASTMTP ELCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPR174 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)
- 0.3
- Highest tissue expression
- 16 nTPM
Expression across tissuesHPA
Tissue
- thymus: 16 nTPM
- lymph node: 14 nTPM
- tonsil: 9.8 nTPM
- spleen: 7.7 nTPM
- appendix: 6.5 nTPM
- small intestine: 3.4 nTPM
Single-cell type
- t-cells: 105 nCPM
- nk-cells: 72 nCPM
- thymocytes: 39 nCPM
- b-cells: 34 nCPM
- innate lymphoid cells: 27 nCPM
- pdcs: 18 nCPM
Immune cell
- basophil: 6.8 nTPM
- memory CD8 T-cell: 6 nTPM
- non-classical monocyte: 5.5 nTPM
- naive CD8 T-cell: 4.9 nTPM
- memory CD4 T-cell: 4.8 nTPM
- T-reg: 4.8 nTPM
Brain region
- cerebellum: 2.4 nTPM
- medulla oblongata: 2.4 nTPM
- pons: 2.3 nTPM
- cerebral cortex: 2 nTPM
- amygdala: 1.9 nTPM
- midbrain: 1.9 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)
- 0.68
- gnomAD pLI
- 0.4
- gnomAD missense Z
- 0.65
- DepMap mean gene effect
- 0.1
- DepMap dependency class
- none
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
- G protein-coupled receptor signaling pathway
- negative regulation of interleukin-2 production
- T cell homeostasis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G protein-coupled receptor, rhodopsin-like
- GPCR, rhodopsin-like, 7TM
- 7 transmembrane receptor (rhodopsin family)
- G protein-coupled receptor 174, 7TM
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPR174 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 GPR174 as an antibody target. Whether an autoantibody or antibody against GPR174 could matter depends on whether native GPR174 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPR174 is annotated at the cell surface, where native GPR174 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 GPR174 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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