CLEC12A
C-type lectin domain family 12 member A
Also known as: CD371, CL12A_HUMAN, CLL-1, DCAL-2, MICL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5QGZ9
- Gene
- CLEC12A
- Ensembl
- ENSG00000172322
- Chromosome
- 12
- Canonical length
- 265 aa
- Protein class
- CD markers, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signaling, glycoprotein turnover, and roles in inflammation and immune response. The protein encoded by this gene is a negative regulator of granulocyte and monocyte function. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. This gene is closely linked to other CTL/CTLD superfamily members in the natural killer gene complex region on chromosome 12p13. [provided by RefSeq, May 2011]
Canonical amino-acid sequenceUniProt
265 residues, UniProt reviewed canonical sequence.
>Q5QGZ9|CLEC12A
1 MSEEVTYADL QFQNSSEMEK IPEIGKFGEK APPAPSHVWR PAALFLTLLC LLLLIGLGVL
61 ASMFHVTLKI EMKKMNKLQN ISEELQRNIS LQLMSNMNIS NKIRNLSTTL QTIATKLCRE
121 LYSKEQEHKC KPCPRRWIWH KDSCYFLSDD VQTWQESKMA CAAQNASLLK INNKNALEFI
181 KSQSRSYDYW LGLSPEEDST RGMRVDNIIN SSAWVIRNAP DLNNMYCGYI NRLYVQYYHC
241 TYKKRMICEK MANPVQLGST YFREALocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLEC12A 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
- 75 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 75 nTPM
- spleen: 21 nTPM
- lung: 16 nTPM
- appendix: 13 nTPM
- smooth muscle: 7.2 nTPM
- lymph node: 6.1 nTPM
Single-cell type
- neutrophil progenitors: 806 nCPM
- neutrophils: 461 nCPM
- monocytes: 234 nCPM
- kupffer cells: 182 nCPM
- monocyte progenitors: 160 nCPM
- cdc: 82 nCPM
Immune cell
- eosinophil: 203 nTPM
- classical monocyte: 137 nTPM
- non-classical monocyte: 131 nTPM
- intermediate monocyte: 115 nTPM
- myeloid DC: 73 nTPM
- total PBMC: 62 nTPM
Brain region
- choroid plexus: 4.2 nTPM
- medulla oblongata: 2.8 nTPM
- cerebral cortex: 2.3 nTPM
- pons: 2.2 nTPM
- amygdala: 2.1 nTPM
- basal ganglia: 2.1 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)
- 1.43
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.22
- 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
- negative regulation of dendritic cell differentiation
- negative regulation of immune response
- negative regulation of inflammatory response
- negative regulation of natural killer cell activation
- negative regulation of neutrophil activation
- positive regulation of type I interferon production
- signal transduction
Molecular functions
- carbohydrate binding
- pattern recognition receptor activity
- signaling receptor regulator activity
- transmembrane signaling receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CLEC12A as an antibody target. Whether an autoantibody or antibody against CLEC12A could matter depends on whether native CLEC12A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLEC12A is annotated at the cell surface, where native CLEC12A 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 CLEC12A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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