muscular LMNA-interacting protein isoform X13 [Homo sapiens]

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Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.

A novel MLIP truncating variant in an 80-year-old patient with late-onset progressive weakness. [Brain. 2022]
A novel MLIP truncating variant in an 80-year-old patient with late-onset progressive weakness.
Bermejo-Guerrero L, Arteche-López A, de Fuenmayor Fernández de la Hoz C, Hernández-Laín A, Martín MA, Domínguez-González C. Brain. 2022 Oct 21; 145(10):e99-e102.
Novel homozygous nonsense mutation of MLIP and compensatory alternative splicing. [NPJ Genom Med. 2022]
Novel homozygous nonsense mutation of MLIP and compensatory alternative splicing.
Mezreani J, Audet S, Martin F, Charbonneau J, Triassi V, Bareke E, Laplante A, Karamchandani J, Massie R, Chalk CH, et al. NPJ Genom Med. 2022 Jun 7; 7(1):36. Epub 2022 Jun 7.
Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia. [Eur J Neurol. 2022]
Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia.
Salzer-Sheelo L, Fellner A, Orenstein N, Bazak L, Lev-El Halabi N, Daue M, Smirin-Yosef P, Van Hout CV, Fellig Y, Ruhrman-Shahar N, et al. Eur J Neurol. 2022 Apr; 29(4):1174-1180. Epub 2022 Jan 7.

RefSeq mRNA
See reference mRNA sequence for the MLIP gene (XM_047419511.1).
RefSeq protein isoforms
See 37 reference sequence protein isoforms for the MLIP gene.

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Protein