metabolic syndrome x Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14221)
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29 genes co-occuring with the disease metabolic syndrome x in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
INS insulin 1.25515
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4 0.912257
LEP leptin 0.834378
PPARD peroxisome proliferator-activated receptor delta 0.714811
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1 0.677504
IGFBP4 insulin-like growth factor binding protein 4 0.660404
DBI diazepam binding inhibitor (GABA receptor modulator, acyl-CoA binding protein) 0.644586
IL6 interleukin 6 0.621008
CRP C-reactive protein, pentraxin-related 0.606933
INSR insulin receptor 0.588222
DNAH8 dynein, axonemal, heavy chain 8 0.557509
ACSL1 acyl-CoA synthetase long-chain family member 1 0.535796
PPARG peroxisome proliferator-activated receptor gamma 0.505356
PPARA peroxisome proliferator-activated receptor alpha 0.504973
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 0.47753
GCG glucagon 0.453716
SHBG sex hormone-binding globulin 0.436026
HMGB1 high mobility group box 1 0.419142
GCK glucokinase (hexokinase 4) 0.416521
APOB apolipoprotein B 0.373698
TNF tumor necrosis factor 0.362239
RETN resistin 0.35892
CRH corticotropin releasing hormone 0.32774
SCD stearoyl-CoA desaturase (delta-9-desaturase) 0.32009
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) 0.264785
UCP2 uncoupling protein 2 (mitochondrial, proton carrier) 0.215992
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2 0.204593
APOC3 apolipoprotein C-III 0.178682
MGAM maltase-glucoamylase 0.158778