GNMT


Summary: The protein encoded by this gene is an enzyme that catalyzes the conversion of S-adenosyl-L-methionine (along with glycine) to S-adenosyl-L-homocysteine and sarcosine. This protein is found in the cytoplasm and acts as a homotetramer. Defects in this gene are a cause of GNMT deficiency (hypermethioninemia). Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between the upstream CNPY3 (canopy FGF signaling regulator 3) gene and this gene and is represented with GeneID:107080644. [provided by RefSeq, Jan 2016].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
OMIM IDMIM:606628
PHARMGKB IDPA28794
Map Location6p21.1

GO terms in GNMT


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Term Type
Evidence Type
GO Term ID
GO Des.
CC IDA GO:0005829 cytosol
CC TAS GO:0005829 cytosol
BP IEA GO:0005977 glycogen metabolic process
BP IEA GO:0006111 regulation of gluconeogenesis
BP NAS GO:0006464 cellular protein modification process
BP IEA GO:0006555 methionine metabolic process
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Gene expression in normal tissue: GNMT

Gene-model tissue-cancer distribution: Bubble Plot

Gene-drug pathway distribution

Pathways in GNMT


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Database
Pathway ID
Pathway Des.
wikipathways WP3940 One carbon metabolism and related pathways
smpdb SMP00004 Glycine and Serine Metabolism
smpdb SMP00179 Dihydropyrimidine Dehydrogenase Deficiency (DHPD)
smpdb SMP00223 Non Ketotic Hyperglycinemia
smpdb SMP00242 Dimethylglycine Dehydrogenase Deficiency
smpdb SMP00244 Sarcosinemia
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Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD353 PD0325901 1
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in GNMT

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
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