nonalcoholic fatty liver disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A term referring to fatty replacement of the hepatic parenchyma which is not related to alcohol use. (Experimental Factor Ontology, EFO_0003095)
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19 genes associated with the disease nonalcoholic fatty liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACADL acyl-CoA dehydrogenase, long chain
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein)
CACNA2D1 calcium channel, voltage-dependent, alpha 2/delta subunit 1
COL13A1 collagen, type XIII, alpha 1
CRACR2A calcium release activated channel regulator 2A
EHBP1L1 EH domain binding protein 1-like 1
FARP1 FERM, RhoGEF (ARHGEF) and pleckstrin domain protein 1 (chondrocyte-derived)
FDFT1 farnesyl-diphosphate farnesyltransferase 1
MACROD2 MACRO domain containing 2
MAST4 microtubule associated serine/threonine kinase family member 4
PKDCC protein kinase domain containing, cytoplasmic
PPID peptidylprolyl isomerase D
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
SEL1L3 sel-1 suppressor of lin-12-like 3 (C. elegans)
SLC46A3 solute carrier family 46, member 3
SLC9A9 solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9
ST8SIA1 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
TRIM44 tripartite motif containing 44