Neonatal Hypoglycemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0158986
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Genes

52 genes associated with the disease Neonatal Hypoglycemia 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
AKT2 v-akt murine thymoma viral oncogene homolog 2
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
APPL1 adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1
ASXL2 additional sex combs like transcriptional regulator 2
ATP5F1D ATP synthase F1 subunit delta
BLK BLK proto-oncogene, Src family tyrosine kinase
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CEL carboxyl ester lipase
CLPB ClpB homolog, mitochondrial AAA ATPase chaperonin
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
FBP1 fructose-1,6-bisphosphatase 1
FOXA2 forkhead box A2
GALC galactosylceramidase
GATAD2B GATA zinc finger domain containing 2B
GCK glucokinase (hexokinase 4)
GH1 growth hormone 1
GPC3 glypican 3
GYS2 glycogen synthase 2 (liver)
HADH hydroxyacyl-CoA dehydrogenase
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
HLTF helicase-like transcription factor
HNF1A HNF1 homeobox A
HNF4A hepatocyte nuclear factor 4, alpha
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
IGF2 insulin-like growth factor 2
IGFBP3 insulin-like growth factor binding protein 3
INS insulin
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KDM6A lysine (K)-specific demethylase 6A
KLF11 Kruppel-like factor 11
MLYCD malonyl-CoA decarboxylase
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NEUROD1 neuronal differentiation 1
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
NSD1 nuclear receptor binding SET domain protein 1
PAX4 paired box 4
PCK1 phosphoenolpyruvate carboxykinase 1 (soluble)
PDX1 pancreatic and duodenal homeobox 1
PIGQ phosphatidylinositol glycan anchor biosynthesis, class Q
POMC proopiomelanocortin
POMP proteasome maturation protein
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PROP1 PROP paired-like homeobox 1
TBX19 T-box 19
TRIP11 thyroid hormone receptor interactor 11
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)
WAC WW domain containing adaptor with coiled-coil
ZMPSTE24 zinc metallopeptidase STE24