Reactive Hypoglycemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hypoglycermia following a meal (or more generally, after intake of glucose). (Human Phenotype Ontology, HP_0012051)
External Link https://www.disgenet.org/browser/0/1/0/C0271710
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Genes

23 genes associated with the disease Reactive Hypoglycemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALDOB aldolase B, fructose-bisphosphate
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CRIP1 cysteine-rich protein 1 (intestinal)
EHMT1 euchromatic histone-lysine N-methyltransferase 1
FGF19 fibroblast growth factor 19
GCG glucagon
GLP1R glucagon-like peptide 1 receptor
GLUD1 glutamate dehydrogenase 1
GSR glutathione reductase
HNF1A HNF1 homeobox A
IGF2 insulin-like growth factor 2
IL1B interleukin 1, beta
INS insulin
INSR insulin receptor
MEN1 multiple endocrine neoplasia I
PCSK1 proprotein convertase subtilisin/kexin type 1
PPARA peroxisome proliferator-activated receptor alpha
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
SOD2 superoxide dismutase 2, mitochondrial
TNF tumor necrosis factor
ZC4H2 zinc finger, C4H2 domain containing
ZGLP1 zinc finger, GATA-like protein 1