AMT aminomethyltransferase [ Homo sapiens (human) ]
Source: NCBI Gene (ID 275)
Symbol: AMT
Full name: aminomethyltransferase
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: GCE; GCST; GCVT; NKH
Summary: This gene encodes one of four critical components of the glycine cleavage system. Mutations in this gene have been associated with glycine encephalopathy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
Expression: Ubiquitous expression in kidney (RPKM 16.6), liver (RPKM 14.9) and 25 other tissues
Orthologs: mouse
Gene size: 5696bp
Exon count: 9