decreased liver function Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Reduced ability of the liver to perform its functions. (Human Phenotype Ontology, HP_0001410)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001410
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Genes

16 genes associated with the decreased liver function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PNPLA3 patatin-like phospholipase domain containing 3 2.51602
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13 1.99713
GPLD1 glycosylphosphatidylinositol specific phospholipase D1 1.51005
GGT1 gamma-glutamyltransferase 1 1.46277
C12ORF43 chromosome 12 open reading frame 43 1.41863
JMJD1C jumonji domain containing 1C 1.37994
ST6GALNAC3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 1.12851
CELF2 CUGBP, Elav-like family member 2 1.09906
GOT1 glutamic-oxaloacetic transaminase 1, soluble 1.05066
ADAMTS9 ADAM metallopeptidase with thrombospondin type 1 motif, 9 1.00059
CCDC102B coiled-coil domain containing 102B 0.969142
THSD7B thrombospondin, type I, domain containing 7B 0.942765
RGS5 regulator of G-protein signaling 5 0.942765
GALNT13 polypeptide N-acetylgalactosaminyltransferase 13 0.942765
SLC39A11 solute carrier family 39, member 11 0.899912
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila) 0.899912