MTR

5-Methyltetrahydrofolate-Homocysteine Methyltransferase

This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]

CHROMOSOME 1 MTR 1q43 genetics.jdge.cc

SNPs7

These are a select few set of SNPs chosen to research within MTR to do with the area Folate Metabolism.