K Atp Permanent Neonatal 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/C4321446
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Genes

8 genes associated with the disease K Atp Permanent Neonatal 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
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
FOXP3 forkhead box P3
GCK glucokinase (hexokinase 4)
HNF1A HNF1 homeobox A
INS insulin
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
PTF1A pancreas specific transcription factor, 1a