APOC3 Chromosome 11

Apolipoprotein C3
7 variants 7 Health Risk

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What This Gene Does
This gene encodes a protein component of triglyceride (TG)-rich lipoproteins (TRLs) including very low density lipoproteins (VLDL), high density lipoproteins (HDL) and chylomicrons. The encoded protein plays a role in role in the metabolism of these TRLs through multiple modes. This protein has been shown to promote the secretion of VLDL1, inhibit lipoprotein lipase enzyme activity, and delay catabolism of TRL remnants. Mutations in this gene are associated with low plasma triglyceride levels and reduced risk of ischemic cardiovascular disease, and hyperalphalipoproteinemia, which is characterized by elevated levels of high density lipoprotein (HDL) and HDL cholesterol in human patients. This gene and other related genes comprise an apolipoprotein gene cluster on chromosome 11. [provided by RefSeq, Sep 2017]
Gene Info
Gene Group
Apolipoproteins
Locus Type
gene with protein product
Location
11q23.3
Ensembl
ENSG00000110245
Associated Conditions (8)
Coronary heart disease
Apolipoprotein c-III deficiency
Cardiovascular phenotype
Clear cell carcinoma of kidney
Cervical cancer
Cholesterol-ester transfer protein deficiency
Apolipoprotein C-III
nonglycosylated
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS138326449 Health Risk Conflicting classifications of pathogenicity Coronary heart disease, Apolipoprotein c-III deficiency, Cardiovascular phenotype
RS140621530 Health Risk Conflicting classifications of pathogenicity Coronary heart disease, Apolipoprotein c-III deficiency, Cervical cancer
RS147210663 Health Risk Conflicting classifications of pathogenicity Coronary heart disease, Apolipoprotein c-III deficiency, Cardiovascular phenotype
RS76353203 Health Risk Conflicting classifications of pathogenicity Apolipoprotein c-III deficiency, Coronary heart disease, Cardiovascular phenotype
RS773670132 Health Risk Conflicting classifications of pathogenicity Cardiovascular phenotype, Cardiovascular phenotype
RS121918381 Health Risk Pathogenic Apolipoprotein C-III, nonglycosylated, Apolipoprotein C-III
RS121918382 Health Risk Pathogenic Apolipoprotein c-III deficiency, Apolipoprotein c-III deficiency
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