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Gene : ACSL6 Homo sapiens

Name  ? acyl-CoA synthetase long chain family member 6 Cytological Location  5q31.1
Brief Description  acyl-CoA synthetase long chain family member 6
Description  The protein encoded by this gene catalyzes the formation of acyl-CoA from fatty acids, ATP, and CoA, using magnesium as a cofactor. The encoded protein plays a major role in fatty acid metabolism in the brain. Translocations with the ETV6 gene are causes of myelodysplastic syndrome with basophilia, acute myelogenous leukemia with eosinophilia, and acute eosinophilic leukemia. Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2011]
  • synonyms:
  • HGNC:16496,
  • LACS2,
  • OTTHUMG00000150692,
  • FACL6,
  • KIAA0837,
  • ACS2,
  • ACS2,
  • AB020644,
  • uc063gss.1,
  • NM_015256,
  • ACSL6,
  • LACS5,
  • LACS2,
  • LACS5,
  • LACS 6,
  • FACL6,
  • fatty-acid-Coenzyme A ligase, long-chain 6
  • identifiers:
  • 23305,
  • ENSG00000164398,
  • ACSL6

Genome feature

Region: gene ? Length: 62096  
Location: 5:131949973-132012068 reverse strand Cyto location: 5q31.1

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3740 SNPs

5 Cross References

16 Data Sets

7 Homologues

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97 Rna Seq Results