RecName: Full=Carnitine O-acetyltransferase; Short=Carnitine acetylase - Protein

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Skeletal muscle mitochondrial inertia is associated with carnitine acetyltransferase activity and physical function in humans. [JCI Insight. 2023]
Skeletal muscle mitochondrial inertia is associated with carnitine acetyltransferase activity and physical function in humans.
Mancilla RF, Lindeboom L, Grevendonk L, Hoeks J, Koves TR, Muoio DM, Schrauwen P, Schrauwen-Hinderling V, Hesselink MK. JCI Insight. 2023 Jan 10; 8(1). Epub 2023 Jan 10.
CRAT missense variants cause abnormal carnitine acetyltransferase function in an early-onset case of Leigh syndrome. [Hum Mutat. 2020]
CRAT missense variants cause abnormal carnitine acetyltransferase function in an early-onset case of Leigh syndrome.
Laera L, Punzi G, Porcelli V, Gambacorta N, Trisolini L, Pierri CL, De Grassi A. Hum Mutat. 2020 Jan; 41(1):110-114. Epub 2019 Sep 23.
Carnitine, mitochondrial function and therapy. [Adv Drug Deliv Rev. 2009]
Carnitine, mitochondrial function and therapy.
Zammit VA, Ramsay RR, Bonomini M, Arduini A. Adv Drug Deliv Rev. 2009 Nov 30; 61(14):1353-62. Epub 2009 Aug 26.

RefSeq protein isoforms
See 17 reference sequence protein isoforms for the CRAT gene.

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P43155 [Domain Mapping of Disease Mut...]
P43155
Domain Mapping of Disease Mutations
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Evolutionary Trace of Functional Site [Evolutionary Trace of Functio...]
Evolutionary Trace of Functional Site

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Protein