Homo sapiens lamin A/C (LMNA), transcript variant 3, mRNA

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DNA methylation of the Lamin A/C gene is associated with congenital heart disease. [Birth Defects Res. 2024]
DNA methylation of the Lamin A/C gene is associated with congenital heart disease.
Mukherjee N, Bolin EH, Qasim A, Orloff MS, Lupo PJ, Nembhard WN. Birth Defects Res. 2024 Jul; 116(7):e2381.
Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins. [Int J Mol Sci. 2024]
Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins.
Martínez Olorón P, Alegría I, Cesar S, Del Olmo B, Martínez-Barrios E, Carrera-García L, Natera-de Benito D, Nascimento A, Campuzano O, Sarquella-Brugada G. Int J Mol Sci. 2024 May 27; 25(11). Epub 2024 May 27.
Podocytopathies associated with familial partial lipodystrophy due to LMNA variants: report of two cases. [Arch Endocrinol Metab. 2024]
Podocytopathies associated with familial partial lipodystrophy due to LMNA variants: report of two cases.
Morguetti MJ, Neves PDMM, Korkes I, Padilha WSC, Jorge LB, Watanabe A, Watanabe EH, Malheiros DMAC, Noronha IL, Dib SA, et al. Arch Endocrinol Metab. 2024 May 10; 68:e230204.

RefSeq alternative splicing
See 28 reference mRNA sequence splice variants for the LMNA gene.
RefSeq protein product
See the reference protein sequence for lamin isoform A-delta10 (NP_733822.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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Functional Class
Functional class of the sequence domain architecture
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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