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Gene : AMT Homo sapiens

Name  ? aminomethyltransferase Cytological Location  3p21.31
Brief Description  aminomethyltransferase
description  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]
  • synonyms:
  • GCE,
  • aminomethyltransferase (glycine cleavage system protein T),
  • GCST,
  • NKH,
  • NKH,
  • glycine cleavage system protein T,
  • GCST,
  • HGNC:473,
  • GCVT,
  • D13811,
  • AMT,
  • OTTHUMG00000156847,
  • uc003cww.4,
  • NM_000481
  • identifiers:
  • 275,
  • ENSG00000145020,
  • AMT

Genome feature

Region: gene ? Length: 5901  
Location: 3:49416778-49422678 reverse strand Cyto location: 3p21.31


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

26290 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results