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This gene encodes the cellular 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. Alternative splicing of this gene results in 2 transcript variants encoding 2 different isoforms. Additional transcript variants have been described, but their biological validity has not been determined.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: cytoplasmic serine hydroxymethyltransferase; cytosolic serine hydroxymethyltransferase; Glycine hydroxymethyltransferase; MGC15229; MGC24556; serine hydroxymethyltransferase 1 (soluble); serine hydroxymethyltransferase 2 (mitochondrial); Serine hydroxymethyltransferase, cytosolic; Serine methylase; SHMT
基因别名: CSHMT; MEL-32; SHMT; SHMT1
UniProt ID: (Human) P34896, (Rabbit) P07511
Entrez Gene ID: (Pig) 397181, (Human) 6470, (Rabbit) 100009405