Homo sapiens laminin subunit alpha 2 (LAMA2), transcript variant 1, mR - Nucleotide

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An atypical expression of core α-Dystroglycan and Laminin-α2 in skin fibroblasts of patients with congenital muscular dystrophies. [Mol Biol Rep. 2023]
An atypical expression of core α-Dystroglycan and Laminin-α2 in skin fibroblasts of patients with congenital muscular dystrophies.
Sabry S, Issa MY, Abdel-Hamid MS, Eissa NR, Abdel-Ghafar SF, Ibrahim MM, Zaki MS. Mol Biol Rep. 2023 Aug; 50(8):6373-6379. Epub 2023 Jun 15.
Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients. [Front Neurol. 2023]
Unique genotype-phenotype correlations within LAMA2-related limb girdle muscular dystrophy in Chinese patients.
Huang X, Tan D, Zhang Z, Ge L, Liu J, Ding J, Yang H, Wei C, Chang X, Yuan Y, et al. Front Neurol. 2023; 14:1158094. Epub 2023 May 3.
Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation. [J Neuromuscul Dis. 2023]
Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation.
Camelo CG, Artilheiro MC, Martins Moreno CA, Ferraciolli SF, Serafim Silva AM, Fernandes TR, Lucato LT, Rocha AJ, Reed UC, Zanoteli E. J Neuromuscul Dis. 2023; 10(4):483-492.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the LAMA2 gene (NM_001079823.2).
RefSeq protein product
See the reference protein sequence for laminin subunit alpha-2 isoform a precursor (NP_000417.3).

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Protein sequence from Nucleotide coding region
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txid1479645[Organism:noexp] (1)
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Nucleotide

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Nucleotide