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Gene : ACOX2 Homo sapiens

Name  ? acyl-CoA oxidase 2 Cytological Location  3p14.3
Brief Description  acyl-CoA oxidase 2
Description  The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe cognitive disability, and death in children. [provided by RefSeq, Mar 2009]
  • synonyms:
  • trihydroxycoprostanoyl-CoA oxidase,
  • BRCOX,
  • X95190,
  • HGNC:120,
  • uc003dkl.4,
  • 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase,
  • ACOX2,
  • branched chain acyl-CoA oxidase,
  • BRCOX,
  • CBAS6,
  • acyl-Coenzyme A oxidase 2, branched chain,
  • THCCox,
  • BCOX,
  • acyl-CoA oxidase 2, branched chain,
  • NM_003500,
  • OTTHUMG00000159154,
  • THCCox
  • identifiers:
  • 8309,
  • ENSG00000168306,
  • ACOX2

Genome feature

Region: gene ? Length: 32061  
Location: 3:58505136-58537196 reverse strand Cyto location: 3p14.3

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1 Diseases

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3740 SNPs

5 Cross References

19 Data Sets

13 Homologues

0 Located Features

97 Rna Seq Results