neonatal hypoglycemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001998
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Genes

10 genes associated with the neonatal hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT2 v-akt murine thymoma viral oncogene homolog 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
GYS2 glycogen synthase 2 (liver)
H19 H19, imprinted maternally expressed transcript (non-protein coding)
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
KDM6A lysine (K)-specific demethylase 6A
NSD1 nuclear receptor binding SET domain protein 1
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PROP1 PROP paired-like homeobox 1