Folic Acid Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

32 genes associated with the Folic Acid Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
BHMT betaine--homocysteine S-methyltransferase
CBS cystathionine-beta-synthase
CD320 CD320 molecule
CLYBL citrate lyase beta like
COMT catechol-O-methyltransferase
CUBN cubilin (intrinsic factor-cobalamin receptor)
DHFR dihydrofolate reductase
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
FOLR3 folate receptor 3 (gamma)
FPGS folylpolyglutamate synthase
FUT6 fucosyltransferase 6 (alpha (1,3) fucosyltransferase)
GGH gamma-glutamyl hydrolase (conjugase, folylpolygammaglutamyl hydrolase)
GNMT glycine N-methyltransferase
KRAS Kirsten rat sarcoma viral oncogene homolog
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MUT methylmalonyl CoA mutase
PEMT phosphatidylethanolamine N-methyltransferase
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
RFC1 replication factor C (activator 1) 1, 145kDa
SHMT1 serine hydroxymethyltransferase 1 (soluble)
SLC19A1 solute carrier family 19 (folate transporter), member 1
SLC46A1 solute carrier family 46 (folate transporter), member 1
TAS2R39 taste receptor, type 2, member 39
TCN1 transcobalamin I (vitamin B12 binding protein, R binder family)
TCN2 transcobalamin II
TYMS thymidylate synthetase