Monogenic Diabetes Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3888631
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Genes

28 genes associated with the disease Monogenic Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
BCL2A1 BCL2-related protein A1
BLK BLK proto-oncogene, Src family tyrosine kinase
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CEL carboxyl ester lipase
G6PC2 glucose-6-phosphatase, catalytic, 2
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GATA6 GATA binding protein 6
GCK glucokinase (hexokinase 4)
GCKR glucokinase (hexokinase 4) regulator
GLIS3 GLIS family zinc finger 3
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HNF1A HNF1 homeobox A
HNF1B HNF1 homeobox B
HNF4A hepatocyte nuclear factor 4, alpha
INS insulin
INS-IGF2 INS-IGF2 readthrough
INSR insulin receptor
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KLF11 Kruppel-like factor 11
LMNA lamin A/C
MC4R melanocortin 4 receptor
NEUROD1 neuronal differentiation 1
PAX4 paired box 4
PDX1 pancreatic and duodenal homeobox 1
PPARG peroxisome proliferator-activated receptor gamma
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
TCF7 transcription factor 7 (T-cell specific, HMG-box)