spinal dysraphism Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_1089)
Similar Terms
Downloads & Tools

Genes

60 genes associated with the disease spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AHCY adenosylhomocysteinase
ALDH1L1 aldehyde dehydrogenase 1 family, member L1
ALX1 ALX homeobox 1
AMD1 adenosylmethionine decarboxylase 1
AMT aminomethyltransferase
ATIC 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
BHMT betaine--homocysteine S-methyltransferase
BHMT2 betaine--homocysteine S-methyltransferase 2
CARM1 coactivator-associated arginine methyltransferase 1
CBS cystathionine-beta-synthase
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
COQ3 coenzyme Q3 methyltransferase
CREBBP CREB binding protein
CTH cystathionine gamma-lyase
CUBN cubilin (intrinsic factor-cobalamin receptor)
DHFR dihydrofolate reductase
DNMT1 DNA (cytosine-5-)-methyltransferase 1
DNMT3A DNA (cytosine-5-)-methyltransferase 3 alpha
EP300 E1A binding protein p300
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
FOLR1 folate receptor 1 (adult)
FOLR2 folate receptor 2 (fetal)
FOLR3 folate receptor 3 (gamma)
FPGS folylpolyglutamate synthase
FTCD formimidoyltransferase cyclodeaminase
GAMT guanidinoacetate N-methyltransferase
GART phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase
GGH gamma-glutamyl hydrolase (conjugase, folylpolygammaglutamyl hydrolase)
GNMT glycine N-methyltransferase
ICMT isoprenylcysteine carboxyl methyltransferase
MAT1A methionine adenosyltransferase I, alpha
MAT2A methionine adenosyltransferase II, alpha
MAT2B methionine adenosyltransferase II, beta
MGMT O-6-methylguanine-DNA methyltransferase
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFD2 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTHFS 5,10-methenyltetrahydrofolate synthetase (5-formyltetrahydrofolate cyclo-ligase)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
NAT1 N-acetyltransferase 1 (arylamine N-acetyltransferase)
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
NNMT nicotinamide N-methyltransferase
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PON1 paraoxonase 1
PRMT1 protein arginine methyltransferase 1
PRMT2 protein arginine methyltransferase 2
RFC1 replication factor C (activator 1) 1, 145kDa
RNMT RNA (guanine-7-) methyltransferase
SARDH sarcosine dehydrogenase
SHMT1 serine hydroxymethyltransferase 1 (soluble)
SLC19A1 solute carrier family 19 (folate transporter), member 1
TCN2 transcobalamin II
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TRDMT1 tRNA aspartic acid methyltransferase 1
TYMS thymidylate synthetase