rs2229738
This is a variant in the CPT1A gene that changes a alanine to an threonine.
▶GWAS Catalog Trait Associations (96)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (96)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
omega-6:omega-3 polyunsaturated fatty acid ratio
degree of unsaturation measurement
docosahexaenoic acid measurement
docosahexaenoic acid to total fatty acids percentage
omega-3 polyunsaturated fatty acid measurement
saturated fatty acids to total fatty acids percentage
docosahexaenoic acid measurement, fatty acid amount
body height
free cholesterol to total lipids in small LDL percentage
free cholesterol to total lipids in medium LDL percentage
▶ClinVar annotation
Carnitine palmitoyl transferase 1A deficiency; not specified
View on ClinVar →About CPT1A
The mitochondrial oxidation of long-chain fatty acids is initiated by the sequential action of carnitine palmitoyltransferase I (which is located in the outer membrane and is detergent-labile) and carnitine palmitoyltransferase II (which is located in the inner membrane and is detergent-stable), together with a carnitine-acylcarnitine translocase. CPT I is the key enzyme in the carnitine-dependent transport across the mitochondrial inner membrane and its deficiency results in a decreased rate of fatty acid beta-oxidation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
View all CPT1A variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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