Mthfr

Some articles on mthfr:

Methylenetetrahydrofolate Reductase - Genetics - C677T SNP (Ala222Val)
... The MTHFR nucleotide at position 677 in the gene has two possibilities C (cytosine) or T (thymine) ... (homozygous) are said to have mild MTHFR deficiency ... individuals (heterozygotes) are almost the same as normal individuals because the normal MTHFR can make up for the thermolabile MTHFR ...
Methylenetetrahydrofolate Reductase - Genetics - Compound Heterozygotes
677 and 1298 are different locations however, they are both in the 'same' gene MTHFR ... Some studies have shown that the MTHFR protein in people with the genotype 677CT 1298AC does its job a bit less well than the normal MTHFR ... No, everyone has two MTHFR genes ...
Methylenetetrahydrofolate Reductase - Genetics - A1298C SNP (Glu429Ala)
... At nucleotide 1298 of the MTHFR, there are two possibilities A or C ... In studies of human recombinant MTHFR, the protein encoded by 1298C cannot be distinguished from 1298A in terms of activity, thermolability, FAD release, or the protective effect of 5-methyl-THF ... The C mutation does not appear to affect the MTHFR protein ...
Choline - Role in Humans - Pregnancy and Brain Development
... Additionally, mice that are Mthfr -/- (lacking MTHFR) become choline deficient, suggesting that humans with genetic polymorphisms that alter the functionality of the enzyme may also have choline ... C677T and A1298C polymorphisms in MTHFR and A80C polymorphism in the reduced folate carrier gene have not been found to be significant ...