lipoatrophic diabetes Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes. (Human Disease Ontology, DOID_11712)
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Genes

21 genes co-occuring with the disease lipoatrophic diabetes in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
LEP leptin 1.34504
INS insulin 1.31056
INSR insulin receptor 1.19014
PDE3B phosphodiesterase 3B, cGMP-inhibited 0.897461
PTRF polymerase I and transcript release factor 0.805257
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin) 0.570329
ADRB3 adrenoceptor beta 3 0.491978
FOXO4 forkhead box O4 0.479047
IRS1 insulin receptor substrate 1 0.471089
LPL lipoprotein lipase 0.393746
FOXP2 forkhead box P2 0.317909
UCP2 uncoupling protein 2 (mitochondrial, proton carrier) 0.303781
IRS2 insulin receptor substrate 2 0.290462
PIDD1 p53-induced death domain protein 1 0.257358
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2 0.257005
PPARG peroxisome proliferator-activated receptor gamma 0.222136
C3 complement component 3 0.205585
CCR2 chemokine (C-C motif) receptor 2 0.18472
CAV1 caveolin 1, caveolae protein, 22kDa 0.182666
APOB apolipoprotein B 0.165001
TNF tumor necrosis factor 0.160948