XB-FEAT-5834988: Difference between revisions
imported>Xenbase gene generator No edit summary |
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=acsl6= | =acsl6= | ||
This is the community wiki page for the gene ''acsl6'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''acsl6'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
06/19/2017 | |||
Human name has changed for Entrez Gene: 2182. From acyl-CoA synthetase long-chain family member 4 to acyl-CoA synthetase long chain family member 4 ( removed 1 hyphen) | |||
=recorded synonyms= | |||
acs2; facl6; lacs2; lacs5; lacs 6 | |||
=summary from NCBI= | |||
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] |
Revision as of 07:53, 20 June 2017
acsl6
This is the community wiki page for the gene acsl6 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
06/19/2017 Human name has changed for Entrez Gene: 2182. From acyl-CoA synthetase long-chain family member 4 to acyl-CoA synthetase long chain family member 4 ( removed 1 hyphen)
recorded synonyms
acs2; facl6; lacs2; lacs5; lacs 6
=summary from NCBI=
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]