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SHMT1 gene

serine hydroxymethyltransferase 1

Key facts

Official symbol
SHMT1
Full name
SHMT1
Chromosome
17
Map location
17p11.2
Organism
Homo sapiens
NCBI Gene ID
6470
Also known as
CSHMT, SHMT, hcSHMT

Function summary

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].

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Data source: NCBI Gene · alsesAI Gene Library