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Gene : OXCT1 Homo sapiens

Name  ? 3-oxoacid CoA-transferase 1 Cytological Location  5p13.1
Brief Description  3-oxoacid CoA-transferase 1
Description  This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency. [provided by RefSeq, Jul 2008]
  • synonyms:
  • SCOT,
  • Succinyl-CoA:3-ketoacid-CoA transferase,
  • 3-oxoacid CoA transferase 1,
  • OXCT1,
  • U62961,
  • 3-oxoacid CoA transferase,
  • SCOT,
  • uc003jmn.4,
  • OXCT,
  • OXCT,
  • NM_000436,
  • OTTHUMG00000094783,
  • HGNC:8527
  • identifiers:
  • 5019,
  • ENSG00000083720,
  • OXCT1

Genome feature

Region: gene ? Length: 140471  
Location: 5:41730065-41870535 reverse strand Cyto location: 5p13.1

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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]


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Gene Ontology

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3740 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results