Homo sapiens leucine rich transmembrane and O-methyltransferase domain - Nucleotide

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Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness. [Eur Arch Otorhinolaryngol. 2023]
Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness.
Salame M, Bonnet C, Moctar ECM, Brahim SM, Dedy A, Vetah LA, Veten F, Hamed CT, Petit C, Houmeida A. Eur Arch Otorhinolaryngol. 2023 Sep; 280(9):4057-4063. Epub 2023 Mar 16.
Deep analysis of the LRTOMTc.242G>A variant in non-syndromic hearing loss North African patients and the Berber population: Implications for genetic diagnosis and genealogical studies. [Mol Genet Genomic Med. 2021]
Deep analysis of the LRTOMTc.242G>A variant in non-syndromic hearing loss North African patients and the Berber population: Implications for genetic diagnosis and genealogical studies.
Mosrati MA, Fadhlaoui-Zid K, Benammar-Elgaaied A, Gibriel AA, Ben Said M, Masmoudi S. Mol Genet Genomic Med. 2021 Oct; 9(10):e1810. Epub 2021 Sep 13.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the LRTOMT gene.
RefSeq protein product
See the reference protein sequence for transmembrane O-methyltransferase isoform LRTOMT2b (NP_001138782.1).

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Protein sequence from Nucleotide coding region
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Nucleotide