Lipid Metabolism, Inborn Errors Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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6 genes/proteins associated with the disease Lipid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1 2.88009
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5 2.88009
PRKAG3 protein kinase, AMP-activated, gamma 3 non-catalytic subunit 2.88009
LIPC lipase, hepatic 2.88009
SERAC1 serine active site containing 1 2.88009
DECR1 2,4-dienoyl CoA reductase 1, mitochondrial 2.88009