Seroatlas · Human Serome Atlas

GPR19

Probable G-protein coupled receptor 19

Also known as: GPR19_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q15760
Gene
GPR19
Ensembl
ENSG00000183150
Chromosome
12
Canonical length
415 aa
Protein class
G-protein coupled receptors, Predicted intracellular proteins, Predicted membrane proteins

OverviewNCBI Gene

Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Located in cilium. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

415 residues, UniProt reviewed canonical sequence.

>Q15760|GPR19
     1  MVFAHRMDNS KPHLIIPTLL VPLQNRSCTE TATPLPSQYL MELSEEHSWM SNQTDLHYVL
    61  KPGEVATASI FFGILWLFSI FGNSLVCLVI HRSRRTQSTT NYFVVSMACA DLLISVASTP
   121  FVLLQFTTGR WTLGSATCKV VRYFQYLTPG VQIYVLLSIC IDRFYTIVYP LSFKVSREKA
   181  KKMIAASWVF DAGFVTPVLF FYGSNWDSHC NYFLPSSWEG TAYTVIHFLV GFVIPSVLII
   241  LFYQKVIKYI WRIGTDGRTV RRTMNIVPRT KVKTIKMFLI LNLLFLLSWL PFHVAQLWHP
   301  HEQDYKKSSL VFTAITWISF SSSASKPTLY SIYNANFRRG MKETFCMSSM KCYRSNAYTI
   361  TTSSRMAKKN YVGISEIPSM AKTITKDSIY DSFDREAKEK KLAWPINSNP PNTFV

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against GPR19 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)
0.4
Highest tissue expression
7.8 nTPM

Expression across tissuesHPA

Tissue

  • cerebellum: 7.8 nTPM
  • pituitary gland: 7.4 nTPM
  • basal ganglia: 6.9 nTPM
  • hypothalamus: 6.8 nTPM
  • spinal cord: 5.8 nTPM
  • amygdala: 5.1 nTPM

Single-cell type

  • early primary spermatocytes: 29 nCPM
  • somatotrophs: 26 nCPM
  • lactotrophs: 26 nCPM
  • brain excitatory neurons: 21 nCPM
  • brain inhibitory neurons: 21 nCPM
  • oligodendrocyte progenitor cells: 20 nCPM

Immune cell

  • T-reg: 6.4 nTPM
  • neutrophil: 2.9 nTPM
  • memory CD4 T-cell: 2.4 nTPM
  • memory CD8 T-cell: 1.4 nTPM
  • gdT-cell: 1.2 nTPM
  • naive CD8 T-cell: 0.9 nTPM

Brain region

  • hypothalamus: 13 nTPM
  • cerebellum: 13 nTPM
  • cerebral cortex: 8.8 nTPM
  • basal ganglia: 8.6 nTPM
  • thalamus: 8.6 nTPM
  • spinal cord: 8.3 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
0.1
gnomAD missense Z
1.45
DepMap mean gene effect
-0.02
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads GPR19 as an antibody target. Whether an autoantibody or antibody against GPR19 could matter depends on whether native GPR19 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

GPR19 is annotated at the cell surface, where native GPR19 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 GPR19 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/GPR19. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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