abnormal circulating homocysteine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant amount in the blood of sulfur-containing alpha-amino acid found in the plasma; blood levels are regulated by folic acid, vitamin B6 and vitamin B12 (Mammalian Phenotype Ontology, MP_0006076)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006076
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Genes

8 gene mutations causing the abnormal circulating homocysteine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
CBS cystathionine-beta-synthase
CD320 CD320 molecule
CTH cystathionine gamma-lyase
FOLR1 folate receptor 1 (adult)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
SLC46A1 solute carrier family 46 (folate transporter), member 1