SHMT1

Serine Hydroxymethyltransferase 1

This gene encodes the cytosolic form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one-carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. A pseudogene of this gene is located on the short arm of chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

CHROMOSOME 17 SHMT1 17p11.2 genetics.jdge.cc

SNPs1

These are a select few set of SNPs chosen to research within SHMT1 to do with the area Folate Metabolism.