Shmt1 Gene Search Result

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2 records found for search term Shmt1

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1323770	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 ... (more) , 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]	17	18327873	18363550	Human	298	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
1350866	SHMT1P1	SHMT1 pseudogene 1		1	43849421	43851952	Human		symbol , COSMIC , name , Human Proteome Map , old_gene_symbol	gene, pseudo, INFERRED [RefSeq]