Glucosephosphate Dehydrogenase Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH). (Human Disease Ontology, DOID_2862)
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Genes

21 genes associated with the Glucosephosphate Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
ADCY9 adenylate cyclase 9
ANXA2 annexin A2
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
G6PD glucose-6-phosphate dehydrogenase
HBA1 hemoglobin, alpha 1
HBB hemoglobin, beta
HP haptoglobin
IFNG interferon, gamma
IL10 interleukin 10
IL6 interleukin 6
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS2 nitric oxide synthase 2, inducible
SLCO1B1 solute carrier organic anion transporter family, member 1B1
SLCO6A1 solute carrier organic anion transporter family, member 6A1
TEK TEK tyrosine kinase, endothelial
TGFB1 transforming growth factor, beta 1
TGFBR3 transforming growth factor, beta receptor III
TNF tumor necrosis factor
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1