GPR15LG
Protein GPR15LG
Also known as: AP-57, C10orf99, CSBF, FLJ21763, GP15L_HUMAN, GPR15L, RLLV1833, UNQ1833
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UWK7
- Gene
- GPR15LG
- Ensembl
- ENSG00000188373
- Chromosome
- 10
- Canonical length
- 81 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Enables chemokine activity. Involved in several processes, including defense response to other organism; mast cell degranulation; and negative regulation of cell cycle G1/S phase transition. Located in extracellular region. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
81 residues, UniProt reviewed canonical sequence.
>Q6UWK7|GPR15LG
1 MRLLVLSSLL CILLLCFSIF STEGKRRPAK AWSGRRTRLC CHRVPSPNST NLKGHHVRLC
61 KPCKLEPEPR LWVVPGALPQ VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPR15LG 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.61
- Highest tissue expression
- 258 nTPM
Expression across tissuesHPA
Tissue
- rectum: 258 nTPM
- colon: 251 nTPM
- esophagus: 205 nTPM
- vagina: 123 nTPM
- cervix: 94 nTPM
- skin: 40 nTPM
Single-cell type
- esophageal suprabasal cells: 2,234 nCPM
- colonocytes: 963 nCPM
- esophageal apical cells: 627 nCPM
- esophageal basal cells: 400 nCPM
- enteric transient amplifying cells: 394 nCPM
- enterocytes: 328 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
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 nTPM
- hippocampal formation: 0 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)
- 1.49
- gnomAD pLI
- 0.21
- DepMap mean gene effect
- 0.08
- 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
- defense response to fungus
- defense response to Gram-positive bacterium
- G protein-coupled receptor signaling pathway
- lymphocyte chemotaxis
- mast cell degranulation
- negative regulation of cell cycle G1/S phase transition
- negative regulation of cell division
- regulation of keratinocyte proliferation
- regulation of T cell migration
- T cell homeostasis
- T cell migration
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- G-protein coupled receptor ligand 15
- G-protein coupled receptor ligand 15
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPR15LG 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 GPR15LG as an antibody target. Whether an autoantibody or antibody against GPR15LG could matter depends on whether native GPR15LG is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPR15LG is annotated as secreted, so native GPR15LG circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label GPR15LG as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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