GPR85
Probable G-protein coupled receptor 85
Also known as: GPR85_HUMAN, SREB2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P60893
- Gene
- GPR85
- Ensembl
- ENSG00000164604
- Chromosome
- 7
- Canonical length
- 370 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
Members of the G protein-coupled receptor (GPCR) family, such as GPR85, have a similar structure characterized by 7 transmembrane domains. Activation of GPCRs by extracellular stimuli, such as neurotransmitters, hormones, or light, induces an intracellular signaling cascade mediated by heterotrimeric GTP-binding proteins, or G proteins (Matsumoto et al., 2000 [PubMed 10833454]).[supplied by OMIM, Aug 2008]
Canonical amino-acid sequenceUniProt
370 residues, UniProt reviewed canonical sequence.
>P60893|GPR85
1 MANYSHAADN ILQNLSPLTA FLKLTSLGFI IGVSVVGNLL ISILLVKDKT LHRAPYYFLL
61 DLCCSDILRS AICFPFVFNS VKNGSTWTYG TLTCKVIAFL GVLSCFHTAF MLFCISVTRY
121 LAIAHHRFYT KRLTFWTCLA VICMVWTLSV AMAFPPVLDV GTYSFIREED QCTFQHRSFR
181 ANDSLGFMLL LALILLATQL VYLKLIFFVH DRRKMKPVQF VAAVSQNWTF HGPGASGQAA
241 ANWLAGFGRG PTPPTLLGIR QNANTTGRRR LLVLDEFKME KRISRMFYIM TFLFLTLWGP
301 YLVACYWRVF ARGPVVPGGF LTAAVWMSFA QAGINPFVCI FSNRELRRCF STTLLYCRKS
361 RLPREPYCVILocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPR85 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)
- 0.33
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 30 nTPM
- basal ganglia: 19 nTPM
- hippocampal formation: 16 nTPM
- midbrain: 14 nTPM
- hypothalamus: 12 nTPM
- cerebral cortex: 12 nTPM
Single-cell type
- late primary spermatocytes: 201 nCPM
- early spermatids: 187 nCPM
- hofbauer cells: 88 nCPM
- retinal horizontal cells: 74 nCPM
- retinal amacrine cells: 62 nCPM
- retinal bipolar cells: 60 nCPM
Immune cell
- basophil: 0.6 nTPM
- intermediate monocyte: 0.4 nTPM
- non-classical monocyte: 0.4 nTPM
- neutrophil: 0.3 nTPM
- classical monocyte: 0.2 nTPM
- eosinophil: 0.2 nTPM
Brain region
- hippocampal formation: 36 nTPM
- cerebral cortex: 33 nTPM
- white matter: 31 nTPM
- amygdala: 30 nTPM
- pons: 29 nTPM
- basal ganglia: 27 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)
- 0.51
- gnomAD pLI
- 0.77
- gnomAD missense Z
- 2.05
- DepMap mean gene effect
- 0.03
- 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
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPR85 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 GPR85 as an antibody target. Whether an autoantibody or antibody against GPR85 could matter depends on whether native GPR85 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPR85 is annotated at the cell surface, where native GPR85 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 GPR85 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...