familial hypertriglyceridemia Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A lipid metabolism disorder characterized by elevated triglyceride levels as a result of excess hepatic production of VLDL or heterozygous LPL deficiency. (Human Disease Ontology, DOID_0050527)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0050527
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Genes

7 genes associated with the disease familial hypertriglyceridemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
GCKR glucokinase (hexokinase 4) regulator 1.7256
TMEM241 transmembrane protein 241 1.39396
TBL2 transducin (beta)-like 2 1.14463
HAVCR1 hepatitis A virus cellular receptor 1 1.10764
BAZ1B bromodomain adjacent to zinc finger domain, 1B 1.10764
FAN1 FANCD2/FANCI-associated nuclease 1 1.02476
PHYHIP phytanoyl-CoA 2-hydroxylase interacting protein 1.00407