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Gene : ACAD9 Homo sapiens

Name  ? acyl-CoA dehydrogenase family member 9 Cytological Location  3q21.3
Brief Description  acyl-CoA dehydrogenase family member 9
Description  This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
  • synonyms:
  • acyl-Coenzyme A dehydrogenase family, member 9,
  • MGC14452,
  • MC1DN20,
  • uc003ela.5,
  • NM_014049,
  • AF078854,
  • acyl-CoA dehydrogenase family, member 9,
  • OTTHUMG00000159942,
  • NPD002,
  • NPD002,
  • HGNC:21497,
  • ACAD9
  • identifiers:
  • 28976,
  • ENSG00000177646,
  • ACAD9

Genome feature

Region: gene ? Length: 33519  
Location: 3:128879596-128913114 Cyto location: 3q21.3

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Gene -> HPO annotation (Human Phenotype Ontology)

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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(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3740 SN Ps

5 Cross References

17 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results