| Name |
|---|
HCHOLA4 Genehypercholesterolemia, autosomal dominant 4 |
OPHLC GeneOmphalocele due to duplication of 1p31.3 |
PSHK2 GenePseudohyperkalemia, familial, 2, due to red cell leak |
SM2 GeneHepatic fibrosis susceptibility due to Schistosoma mansoni infection |
HDLCQ6 GeneHigh density lipoprotein cholesterol level QTL 6 |
HDLCQ1 Genehigh density lipoprotein cholesterol level QTL 1 |
CLQTL1 Genecholesterol-lowering factor |
CLQTL2 GeneCholesterol level QTL 2 |
NCEH1 Geneneutral cholesterol ester hydrolase 1 Predicted to enable serine hydrolase activity. Predicted to be involved in ether lipid metabolic process. Predicted to act upstream of or within protein dephosphorylation and xenobiotic metabolic process. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LIPA Genelipase A, lysosomal acid, cholesterol esterase This gene encodes lipase A, the lysosomal acid lipase (also known as cholesterol ester hydrolase). This enzyme functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides. Mutations in this gene can result in Wolman disease and cholesteryl ester storage disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2014] |
LCAT Genelecithin-cholesterol acyltransferase This gene encodes the extracellular cholesterol esterifying enzyme, lecithin-cholesterol acyltransferase. The esterification of cholesterol is required for cholesterol transport. Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency. [provided by RefSeq, Jul 2008] |
HDLCQ4 GeneHigh density lipoprotein cholesterol level QTL 4 |
HDLCQ5 GeneHigh density lipoprotein cholesterol level QTL 5 |
HDLCQ2 GeneHigh density lipoprotein cholesterol level QTL on chromosome 8 |
HDLC3 GeneHigh density lipoprotein cholesterol, low serum, 3 |
CHROMR Genecholesterol induced regulator of metabolism RNA |