PREDICTED: Homo sapiens dystrobrevin alpha (DTNA), transcript variant - Nucleotide

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Variants in DTNA cause a mild, dominantly inherited muscular dystrophy. [Acta Neuropathol. 2023]
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy.
Nascimento A, Bruels CC, Donkervoort S, Foley AR, Codina A, Milisenda JC, Estrella EA, Li C, Pijuan J, Draper I, et al. Acta Neuropathol. 2023 Apr; 145(4):479-496. Epub 2023 Feb 17.
Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity. [Mol Cell. 2023]
Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity.
Golkowski M, Lius A, Sapre T, Lau HT, Moreno T, Maly DJ, Ong SE. Mol Cell. 2023 Mar 2; 83(5):803-818.e8. Epub 2023 Feb 2.
O-GlcNAcylation of SPOP promotes carcinogenesis in hepatocellular carcinoma. [Oncogene. 2023]
O-GlcNAcylation of SPOP promotes carcinogenesis in hepatocellular carcinoma.
Zhou P, Chang WY, Gong DA, Huang LY, Liu R, Liu Y, Xia J, Wang K, Tang N, Huang AL. Oncogene. 2023 Mar; 42(10):725-736. Epub 2023 Jan 5.

RefSeq alternative splicing
See 96 reference mRNA sequence splice variants for the DTNA gene.
RefSeq protein product
See the reference protein sequence for dystrobrevin alpha isoform X11 (XP_054174225.1).

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Protein sequence from Nucleotide coding region
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Hearing Loss, Functional
Hearing Loss, Functional
Hearing loss without a physical basis. Often observed in patients with psychological or behavioral disorders.<br/>Year introduced: 1991(1979)

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Nucleotide