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Gene : AGXT Homo sapiens

Name  ? alanine--glyoxylate and serine--pyruvate aminotransferase Cytological Location  2q37.3
Brief Description  alanine-glyoxylate 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:
  • NM_000030,
  • uc002waa.5,
  • AGT,
  • D13368,
  • L-alanine: glyoxylate aminotransferase 1,
  • SPAT,
  • HGNC:341,
  • serine:pyruvate aminotransferase,
  • alanine-glyoxylate aminotransferase,
  • PH1,
  • AGT1,
  • SPT,
  • AGT1,
  • oxalosis I,
  • AGXT,
  • SPAT,
  • SPT,
  • PH1,
  • TLH6,
  • glycolicaciduria,
  • AGXT1,
  • AGXT1,
  • primary hyperoxaluria type 1,
  • OTTHUMG00000133354,
  • AGT
  • identifiers:
  • 189,
  • ENSG00000172482,
  • AGXT

Genome feature

Region: gene ? Length: 10375  
Location: 2:240868745-240879119 Cyto location: 2q37.3


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Disease

1 Diseases

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605 SN Ps

5 Cross References

20 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results