lecithin:retinol acyltransferase isoform 1 [Homo sapiens]

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A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa. [Hum Genomics. 2018]
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa.
Chen Y, Huang L, Jiao X, Riazuddin S, Riazuddin SA, Fielding Hetmancik J. Hum Genomics. 2018 Jul 4; 12(1):35. Epub 2018 Jul 4.
A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia. [J Clin Lipidol. 2017]
A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia.
Rial-Crestelo D, Santos-Recuero I, Julve J, Blanco-Vaca F, Torralba M. J Clin Lipidol. 2017 Nov-Dec; 11(6):1475-1479.e3. Epub 2017 Aug 24.
High incidence of LRAT promoter hypermethylation in colorectal cancer correlates with tumor stage. [Med Oncol. 2014]
High incidence of LRAT promoter hypermethylation in colorectal cancer correlates with tumor stage.
Cheng YW, Pincas H, Huang J, Zachariah E, Zeng Z, Notterman DA, Paty P, Barany F. Med Oncol. 2014 Nov; 31(11):254. Epub 2014 Sep 27.

RefSeq genomic sequence
See the genomic reference sequence for the LRAT gene (NG_009110.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the LRAT gene.

Nucleotide
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Transcript/Protein Information [PANTHER Classification System]
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PANTHER Classification System
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
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Protein