GPR162
Probable G-protein coupled receptor 162
Also known as: A-2, GP162_HUMAN, GRCA
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16538
- Gene
- GPR162
- Ensembl
- ENSG00000250510
- Chromosome
- 12
- Canonical length
- 588 aa
- Protein class
- G-protein coupled receptors, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Centriolar satellite
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
This gene was identified upon genomic analysis of a gene-dense region at human chromosome 12p13. It appears to be mainly expressed in the brain; however, its function is not known. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
588 residues, UniProt reviewed canonical sequence.
>Q16538|GPR162
1 MARGGAGAEE ASLRSNALSW LACGLLALLA NAWIILSISA KQQKHKPLEL LLCFLAGTHI
61 LMAAVPLTTF AVVQLRRQAS SDYDWNESIC KVFVSTYYTL ALATCFTVAS LSYHRMWMVR
121 WPVNYRLSNA KKQALHAVMG IWMVSFILST LPSIGWHNNG ERYYARGCQF IVSKIGLGFG
181 VCFSLLLLGG IVMGLVCVAI TFYQTLWARP RRARQARRVG GGGGTKAGGP GALGTRPAFE
241 VPAIVVEDAR GKRRSSLDGS ESAKTSLQVT NLVSAIVFLY DSLTGVPILV VSFFSLKSDS
301 APPWMVLAVL WCSMAQTLLL PSFIWSCERY RADVRTVWEQ CVAIMSEEDG DDDGGCDDYA
361 EGRVCKVRFD ANGATGPGSR DPAQVKLLPG RHMLFPPLER VHYLQVPLSR RLSHDETNIF
421 STPREPGSFL HKWSSSDDIR VLPAQSRALG GPPEYLGQRH RLEDEEDEEE AEGGGLASLR
481 QFLESGVLGS GGGPPRGPGF FREEITTFID ETPLPSPTAS PGHSPRRPRP LGLSPRRLSL
541 GSPESRAVGL PLGLSAGRRC SLTGGEESAR AWGGSWGPGN PIFPQLTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPR162 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)
- 0.48
- Highest tissue expression
- 144 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 144 nTPM
- cerebral cortex: 120 nTPM
- hippocampal formation: 100 nTPM
- choroid plexus: 73 nTPM
- amygdala: 70 nTPM
- hypothalamus: 65 nTPM
Single-cell type
- respiratory ciliated cells: 114 nCPM
- fallopian tube ciliated cells: 69 nCPM
- ependymal cells: 59 nCPM
- retinal amacrine cells: 55 nCPM
- retinal bipolar cells: 48 nCPM
- brain excitatory neurons: 44 nCPM
Immune cell
- neutrophil: 18 nTPM
- classical monocyte: 6.9 nTPM
- intermediate monocyte: 4.3 nTPM
- myeloid DC: 2 nTPM
- total PBMC: 1.9 nTPM
- plasmacytoid DC: 1.7 nTPM
Brain region
- cerebral cortex: 139 nTPM
- hippocampal formation: 131 nTPM
- white matter: 85 nTPM
- basal ganglia: 85 nTPM
- cerebellum: 75 nTPM
- amygdala: 74 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)
- 0.66
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.89
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GPR162 as an antibody target. Whether an autoantibody or antibody against GPR162 could matter depends on whether native GPR162 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPR162 is annotated at the cell surface, where native GPR162 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 GPR162 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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