help  | about  | cite  | software

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:
  • D13811,
  • glycine cleavage system protein T,
  • uc003cww.4,
  • GCST,
  • nonketotic hyperglycinemia,
  • GCST,
  • AMT,
  • GCE,
  • HGNC:473,
  • NKH,
  • GCVT,
  • NKH,
  • NM_000481,
  • aminomethyltransferase (glycine cleavage system protein T),
  • OTTHUMG00000156847
  • identifiers:
  • 275,
  • ENSG00000145020,
  • AMT

Genome feature

Region: gene ? Length: 5696  
Location: 3:49416778-49422473 reverse strand Cyto location: 3p21.31

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


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]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



45921 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results