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Gene : ACAD8 Homo sapiens

Name  ? acyl-CoA dehydrogenase family member 8 Cytological Location  11q25
Brief Description  acyl-CoA dehydrogenase family member 8
description  This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. The encoded protein is a mitochondrial enzyme that functions in catabolism of the branched-chain amino acid valine. Defects in this gene are the cause of isobutyryl-CoA dehydrogenase deficiency.[provided by RefSeq, Nov 2009]
  • synonyms:
  • uc001qhk.4,
  • HGNC:87,
  • OTTHUMG00000167177,
  • NM_014384,
  • ARC42,
  • ACAD8,
  • isobutyryl-CoA dehydrogenase,
  • ACAD-8,
  • acyl-Coenzyme A dehydrogenase family, member 8,
  • AF126245,
  • acyl-CoA dehydrogenase family, member 8
  • identifiers:
  • 27034,
  • ENSG00000151498,
  • ACAD8

Genome feature

Region: gene ? Length: 12321  
Location: 11:134253538-134265858 Cyto location: 11q25


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Genomics

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Proteins

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SNPs

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Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Gene -> HPO annotation (Human Phenotype Ontology)

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Homology

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Expression

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Other

294 SN Ps

5 Cross References

19 Data Sets

3 Homologues

0 Located Features

90 Rna Seq Results