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Gene : ACSF3 Homo sapiens

Name  ? acyl-CoA synthetase family member 3 Cytological Location  16q24.3
Brief Description  acyl-CoA synthetase family member 3
description  This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Sep 2013]
  • synonyms:
  • OTTHUMG00000138044,
  • ACSF3,
  • malonyl-CoA synthetase,
  • NM_174917,
  • uc021tmq.2,
  • HGNC:27288,
  • AK075499
  • identifiers:
  • 197322,
  • ENSG00000176715,
  • ACSF3

Genome feature

Region: gene ? Length: 66748  
Location: 16:89093809-89160556 Cyto location: 16q24.3


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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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Expression

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2011 SN Ps

5 Cross References

16 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results