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Gene : GNMT Homo sapiens

Name  ? glycine N-methyltransferase Cytological Location  6p21.1
Brief Description  glycine N-methyltransferase
description  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]
  • synonyms:
  • HGNC:4415,
  • GNMT,
  • uc003otd.4,
  • AF101475,
  • OTTHUMG00000014712,
  • NM_018960,
  • HEL-S-182mP
  • identifiers:
  • 27232,
  • ENSG00000124713,
  • GNMT

Genome feature

Region: gene ? Length: 3127  
Location: 6:42960754-42963880 Cyto location: 6p21.1


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Proteins

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SNPs

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Disease

1 Diseases

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Expression

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2011 SN Ps

5 Cross References

19 Data Sets

5 Homologues

0 Located Features

90 Rna Seq Results