Metabolic Syndrome X Gene Set

Dataset dbGAP Gene-Trait Associations
Category disease or phenotype associations
Type trait
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14221)
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23 genes associated with the trait Metabolic Syndrome X in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol Name Standardized Value
ZPR1 ZPR1 zinc finger 1.69671
G6PC2 glucose-6-phosphatase, catalytic, 2 1.58259
GCKR glucokinase (hexokinase 4) regulator 1.39727
APOA5 apolipoprotein A-V 1.26538
BUD13 BUD13 homolog (S. cerevisiae) 1.24151
LPL lipoprotein lipase 1.0562
CETP cholesteryl ester transfer protein, plasma 1.02473
MLXIPL MLX interacting protein-like 0.995026
CAMK2B calcium/calmodulin-dependent protein kinase II beta 0.947427
APOB apolipoprotein B 0.944178
EDC4 enhancer of mRNA decapping 4 0.922056
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1 0.88185
CCDC121 coiled-coil domain containing 121 0.862644
GPN1 GPN-loop GTPase 1 0.862644
NR1H3 nuclear receptor subfamily 1, group H, member 3 0.862644
C2ORF16 chromosome 2 open reading frame 16 0.836775
FTO fat mass and obesity associated 0.836775
ZNF512 zinc finger protein 512 0.796965
TOMM40 translocase of outer mitochondrial membrane 40 homolog (yeast) 0.763999
SMEK2 SMEK homolog 2, suppressor of mek1 (Dictyostelium) 0.696869
GALNT2 polypeptide N-acetylgalactosaminyltransferase 2 0.696869
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11 0.654022
TFAP2B transcription factor AP-2 beta (activating enhancer binding protein 2 beta) 0.64828