CLEC4C
C-type lectin domain family 4 member C
Also known as: BDCA2, CD303, CLC4C_HUMAN, CLECSF11, CLECSF7, DLEC, HECL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8WTT0
- Gene
- CLEC4C
- Ensembl
- ENSG00000198178
- Chromosome
- 12
- Canonical length
- 213 aa
- Protein class
- CD markers, 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 2 transmembrane protein may play a role in dendritic cell function. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
213 residues, UniProt reviewed canonical sequence.
>Q8WTT0|CLEC4C
1 MVPEEEPQDR EKGLWWFQLK VWSMAVVSIL LLSVCFTVSS VVPHNFMYSK TVKRLSKLRE
61 YQQYHPSLTC VMEGKDIEDW SCCPTPWTSF QSSCYFISTG MQSWTKSQKN CSVMGADLVV
121 INTREEQDFI IQNLKRNSSY FLGLSDPGGR RHWQWVDQTP YNENVTFWHS GEPNNLDERC
181 AIINFRSSEE WGWNDIHCHV PQKSICKMKK IYILocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLEC4C 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)
- 0.34
- Highest tissue expression
- 5.1 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 5.1 nTPM
- tonsil: 4.9 nTPM
- spleen: 3.6 nTPM
- thymus: 1.9 nTPM
- bone marrow: 1.4 nTPM
- appendix: 1.3 nTPM
Single-cell type
- pdcs: 423 nCPM
- oocytes: 101 nCPM
- undifferentiated spermatogonia: 27 nCPM
- differentiating spermatogonia: 20 nCPM
- cdc: 7.4 nCPM
- thymocytes: 5.1 nCPM
Immune cell
- plasmacytoid DC: 469 nTPM
- eosinophil: 30 nTPM
- neutrophil: 15 nTPM
- basophil: 5.3 nTPM
- myeloid DC: 4.1 nTPM
- NK-cell: 3 nTPM
Brain region
- choroid plexus: 2.5 nTPM
- cerebellum: 1.6 nTPM
- cerebral cortex: 1.3 nTPM
- white matter: 1.1 nTPM
- basal ganglia: 1 nTPM
- hippocampal formation: 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)
- 1.32
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.7
- DepMap mean gene effect
- 0.05
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CLEC4C as an antibody target. Whether an autoantibody or antibody against CLEC4C could matter depends on whether native CLEC4C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLEC4C is annotated at the cell surface, where native CLEC4C 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 CLEC4C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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