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GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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CLEC4M
C-type lectin domain family 4 member M
Chromosome 19 · 19p13.2
NCBI Gene: 10332Ensembl: ENSG00000104938.18HGNC: HGNC:13523UniProt: A0A7P0MMK7
131PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Receptor
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
virus receptor activitycalcium-dependent protein bindingsymbiont entry into host cellreceptor-mediated virion attachment to host cellvenous thromboembolismcoronary artery diseaseIschemic strokehepatocellular carcinoma
✦AI Summary

CLEC4M (C-type lectin domain family 4 member M) is a cell surface receptor that functions primarily in pathogen recognition and coagulation regulation. As a C-type lectin, CLEC4M serves as a pathogen recognition receptor that can bind various pathogens including SARS-CoV-2, functioning as an ACE2-independent alternative receptor for viral entry 1. The protein recognizes mannose-containing glycans and plays a critical role in coagulation factor homeostasis by serving as a clearance receptor for factor VIII (FVIII) through both von Willebrand factor (VWF)-dependent and independent mechanisms 2. CLEC4M mediates FVIII internalization via clathrin-coated pits, leading to lysosomal degradation 2. Genetic variations in CLEC4M significantly influence VWF levels in type 1 von Willebrand disease patients and affect coagulation factor levels in healthy populations 34. The gene contains a highly polymorphic variable number tandem repeat (VNTR) region that evolved before human migration out of Africa and may influence disease susceptibility 5. Clinical studies have identified associations between CLEC4M polymorphisms and COVID-19 severity, with the rs868875 variant linked to more severe outcomes in patients receiving anticoagulants 6. Additionally, CLEC4M expression levels are elevated in lung cancer patients and may serve as a biomarker for platinum chemotherapy resistance 7.

⚠Limited data available — This gene has 0 indexed publications. Summary and analysis may be incomplete.
Disease Associationsⓘ20
venous thromboembolismOpen Targets
0.35Weak
coronary artery diseaseOpen Targets
0.28Weak
Ischemic strokeOpen Targets
0.28Weak
hepatocellular carcinomaOpen Targets
0.13Weak
infectionOpen Targets
0.11Weak
contact dermatitisOpen Targets
0.09Suggestive
non-small cell lung carcinomaOpen Targets
0.09Suggestive
colon carcinomaOpen Targets
0.08Suggestive
neoplasmOpen Targets
0.08Suggestive
lung cancerOpen Targets
0.08Suggestive
Autosomal recessive hyper-IgE syndromeOpen Targets
0.08Suggestive
isolated agammaglobulinemiaOpen Targets
0.08Suggestive
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiencyOpen Targets
0.08Suggestive
immunodeficiency 35Open Targets
0.08Suggestive
gastric cancerOpen Targets
0.08Suggestive
cervical cancerOpen Targets
0.07Suggestive
Immunodeficiency due to a late component of complements deficiencyOpen Targets
0.07Suggestive
immunodeficiency, common variable, 4Open Targets
0.07Suggestive
agammaglobulinemia 8, autosomal dominantOpen Targets
0.07Suggestive
immunodeficiency, common variable, 3Open Targets
0.07Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes

No related genes found for this gene.

Tissue Expression

No tissue expression data available for this gene.

Gene Interaction Network

No interaction data available for this gene.

PROTEIN STRUCTURE
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PDB1XPH · 1.41 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.87LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.61 [0.44–0.87]
RankingsWhere CLEC4M stands among ~20K protein-coding genes
  • #3,552of 20,598
    Most Researched131 · top quartile
  • #7,652of 17,882
    Most Constrained (LOEUF)0.87
Genes detectedCLEC4M
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Levels of APE1 Repair Gene and CLEC4M in Lung Cancer Patients Receiving Cisplatin Chemotherapy.
PMID: 38028841
Arch Razi Inst · 2023
1.00
2
CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease.
PMID: 25832887
J Thromb Haemost · 2015
0.90
3
The origin and evolution of variable number tandem repeat of CLEC4M gene in the global human population.
PMID: 22279577
PLoS One · 2012
0.80
4
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels.
PMID: 38320121
Blood · 2024
0.70
5
Association between single-nucleotide polymorphism rs868875 of CLEC4M gene and clinical severity of COVID-19 in a Brazilian population.
PMID: 41062837
Immunogenetics · 2025
0.60