RecName: Full=Fatty acyl-CoA reductase 1; AltName: Full=Male sterility - Protein

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An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids. [Genet Med. 2021]
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Ferdinandusse S, McWalter K, Te Brinke H, IJlst L, Mooijer PM, Ruiter JPN, van Lint AEM, Pras-Raves M, Wever E, Millan F, et al. Genet Med. 2021 Apr; 23(4):740-750. Epub 2020 Nov 26.
A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency. [Am J Hum Genet. 2014]
A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.
Buchert R, Tawamie H, Smith C, Uebe S, Innes AM, Al Hallak B, Ekici AB, Sticht H, Schwarze B, Lamont RE, et al. Am J Hum Genet. 2014 Nov 6; 95(5):602-10. Epub 2014 Oct 30.
Posttranslational regulation of fatty acyl-CoA reductase 1, Far1, controls ether glycerophospholipid synthesis. [J Biol Chem. 2010]
Posttranslational regulation of fatty acyl-CoA reductase 1, Far1, controls ether glycerophospholipid synthesis.
Honsho M, Asaoku S, Fujiki Y. J Biol Chem. 2010 Mar 19; 285(12):8537-42. Epub 2010 Jan 13.

RefSeq genomic sequence
See the genomic reference sequence for the FAR1 gene (NG_041826.1).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the FAR1 gene.

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Q8WVX9 [Domain Mapping of Disease Mut...]
Q8WVX9
Domain Mapping of Disease Mutations
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