abnormality of homocysteine metabolism Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of a homocysteine metabolic process. (Human Phenotype Ontology, HP_0010919)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0010919
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Genes

19 genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
MTHFR methylenetetrahydrofolate reductase (NAD(P)H) 3.02707
CPS1 carbamoyl-phosphate synthase 1, mitochondrial 2.14121
CBS cystathionine-beta-synthase 2.08559
NOX4 NADPH oxidase 4 1.97023
FANCA Fanconi anemia, complementation group A 1.44286
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase 1.41863
CUBN cubilin (intrinsic factor-cobalamin receptor) 1.36327
TRDMT1 tRNA aspartic acid methyltransferase 1 1.36327
PRDX1 peroxiredoxin 1 1.32793
FGF21 fibroblast growth factor 21 1.26545
SLC17A3 solute carrier family 17 (organic anion transporter), member 3 1.24751
GTPBP10 GTP-binding protein 10 (putative) 1.21853
PTPRD protein tyrosine phosphatase, receptor type, D 0.909447
PLXND1 plexin D1 0.767696
ZBTB16 zinc finger and BTB domain containing 16 0.762459
LAMB1 laminin, beta 1 0.762459
LINC00320 long intergenic non-protein coding RNA 320 0.718314
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.595915
KLK11 kallikrein-related peptidase 11 0.585507