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Gene : AGXT Homo sapiens

Name  ? alanine--glyoxylate and serine--pyruvate aminotransferase Cytological Location  2q37.3
Brief Description  alanine--glyoxylate and serine--pyruvate aminotransferase
Description  This gene is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I primary hyperoxaluria. [provided by RefSeq, Jul 2008]
  • synonyms:
  • AGXT,
  • PH1,
  • AGT,
  • uc002waa.5,
  • AGT1,
  • AGT1,
  • TLH6,
  • AGXT1,
  • SPAT,
  • L-alanine: glyoxylate aminotransferase 1,
  • SPT,
  • SPAT,
  • oxalosis I,
  • NM_000030,
  • alanine-glyoxylate aminotransferase,
  • AGXT1,
  • PH1,
  • glycolicaciduria,
  • SPT,
  • OTTHUMG00000133354,
  • primary hyperoxaluria type 1,
  • AGT,
  • HGNC:341,
  • serine:pyruvate aminotransferase,
  • D13368
  • identifiers:
  • 189,
  • ENSG00000172482,
  • AGXT

Genome feature

Region: gene ? Length: 11677  
Location: 2:240868824-240880500 Cyto location: 2q37.3


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Disease

1 Diseases

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3753 SN Ps

5 Cross References

20 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results