KLRG1
Killer cell lectin-like receptor subfamily G member 1
Also known as: 2F1, CLEC15A, KLRG1_HUMAN, MAFA, MAFA-L
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96E93
- Gene
- KLRG1
- Ensembl
- ENSG00000139187
- Chromosome
- 12
- Canonical length
- 195 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Vesicles
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Natural killer (NK) cells are lymphocytes that can mediate lysis of certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. The protein encoded by this gene belongs to the killer cell lectin-like receptor (KLR) family, which is a group of transmembrane proteins preferentially expressed in NK cells. Studies in mice suggested that the expression of this gene may be regulated by MHC class I molecules. [provided by RefSeq, Jun 2016]
Canonical amino-acid sequenceUniProt
195 residues, UniProt reviewed canonical sequence.
>Q96E93|KLRG1
1 MTDSVIYSML ELPTATQAQN DYGPQQKSSS SRPSCSCLVA IALGLLTAVL LSVLLYQWIL
61 CQGSNYSTCA SCPSCPDRWM KYGNHCYYFS VEEKDWNSSL EFCLARDSHL LVITDNQEMS
121 LLQVFLSEAF CWIGLRNNSG WRWEDGSPLN FSRISSNSFV QTCGAINKNG LQASSCEVPL
181 HWVCKKCPFA DQALFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLRG1 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
- 1
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 9.8 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 9.8 nTPM
- spleen: 8.3 nTPM
- tonsil: 4.7 nTPM
- appendix: 3.6 nTPM
- gallbladder: 3.1 nTPM
- bone marrow: 2.8 nTPM
Single-cell type
- mast cells: 135 nCPM
- t-cells: 98 nCPM
- nk-cells: 72 nCPM
- myonuclei: 57 nCPM
- cardiomyocytes: 45 nCPM
- oligodendrocyte progenitor cells: 33 nCPM
Immune cell
- MAIT T-cell: 462 nTPM
- gdT-cell: 392 nTPM
- memory CD8 T-cell: 238 nTPM
- naive CD8 T-cell: 148 nTPM
- total PBMC: 100 nTPM
- memory CD4 T-cell: 85 nTPM
Brain region
- cerebellum: 14 nTPM
- midbrain: 12 nTPM
- white matter: 12 nTPM
- hypothalamus: 12 nTPM
- cerebral cortex: 11 nTPM
- medulla oblongata: 11 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)
- 1.18
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- 0.14
- 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
- cell surface receptor signaling pathway
- cellular defense response
- inflammatory response
- innate immune response
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- C-type lectin-like
- C-type lectin-like/link domain superfamily
- C-type lectin fold
- Natural killer cell receptor-like, C-type lectin-like domain
- Lectin C-type domain
- Killer cell lectin-like receptor subfamily G member 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KLRG1 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 KLRG1 as an antibody target. Whether an autoantibody or antibody against KLRG1 could matter depends on whether native KLRG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLRG1 is annotated at the cell surface, where native KLRG1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Source-annotated serology context
The source annotations explicitly mention antibody, autoantibody, autoantigen, or autoimmune context. This is biological context, not study-specific reactivity.
- They can also regulate specific humoral and cell-mediated immunity.
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