CLEC4E
C-type lectin domain family 4 member E
Also known as: CLC4E_HUMAN, CLECSF9, MINCLE
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9ULY5
- Gene
- CLEC4E
- Ensembl
- ENSG00000166523
- Chromosome
- 12
- Canonical length
- 219 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- 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 signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type II transmembrane protein is a downstream target of CCAAT/enhancer binding protein (C/EBP), beta (CEBPB) and may play a role in inflammation. Alternative splice variants have been described but their full-length sequence has not been determined. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
219 residues, UniProt reviewed canonical sequence.
>Q9ULY5|CLEC4E
1 MNSSKSSETQ CTERGCFSSQ MFLWTVAGIP ILFLSACFIT RCVVTFRIFQ TCDEKKFQLP
61 ENFTELSCYN YGSGSVKNCC PLNWEYFQSS CYFFSTDTIS WALSLKNCSA MGAHLVVINS
121 QEEQEFLSYK KPKMREFFIG LSDQVVEGQW QWVDGTPLTK SLSFWDVGEP NNIATLEDCA
181 TMRDSSNPRQ NWNDVTCFLN YFRICEMVGI NPLNKGKSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLEC4E 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)
- 0.37
- Highest tissue expression
- 72 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 72 nTPM
- spleen: 51 nTPM
- appendix: 35 nTPM
- lung: 22 nTPM
- choroid plexus: 22 nTPM
- adipose tissue: 12 nTPM
Single-cell type
- neutrophils: 1,575 nCPM
- monocytes: 221 nCPM
- neutrophil progenitors: 134 nCPM
- macrophages: 105 nCPM
- kupffer cells: 104 nCPM
- cdc: 76 nCPM
Immune cell
- neutrophil: 452 nTPM
- classical monocyte: 129 nTPM
- total PBMC: 30 nTPM
- intermediate monocyte: 18 nTPM
- myeloid DC: 17 nTPM
- non-classical monocyte: 0.7 nTPM
Brain region
- cerebral cortex: 14 nTPM
- white matter: 13 nTPM
- hypothalamus: 13 nTPM
- choroid plexus: 13 nTPM
- basal ganglia: 12 nTPM
- hippocampal formation: 12 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)
- 1.29
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.12
- DepMap mean gene effect
- 0.02
- 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
- antifungal innate immune response
- defense response to bacterium
- Fc-gamma receptor signaling pathway
- innate immune response
- pattern recognition receptor signaling pathway
- positive regulation of cytokine production
- T cell differentiation involved in immune response
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CLEC4E 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 CLEC4E as an antibody target. Whether an autoantibody or antibody against CLEC4E could matter depends on whether native CLEC4E is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLEC4E is annotated at the cell surface, where native CLEC4E 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 CLEC4E as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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