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Gene : OAT Homo sapiens

Name  ? ornithine aminotransferase Cytological Location  10q26.13
Brief Description  ornithine aminotransferase
description  This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome. [provided by RefSeq, Jan 2010]
  • synonyms:
  • HOGA,
  • uc001lhp.4,
  • gyrate atrophy,
  • OKT,
  • HOGA,
  • NM_000274,
  • HGNC:8091,
  • GACR,
  • Ornithine aminotransferase,
  • ornithine aminotransferase precursor,
  • BC016928,
  • OTTHUMG00000019213,
  • OAT,
  • identifiers:
  • 4942,
  • ENSG00000065154,
  • OAT

Genome feature

Region: gene ? Length: 21674  
Location: 10:124397303-124418976 reverse strand Cyto location: 10q26.13

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1 Diseases

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744 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results