Homo sapiens lamin A/C (LMNA), RefSeqGene (LRG_254) on chromosome 1

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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.
MEX3A promotes colorectal cancer migration, invasion and EMT via regulating the Wnt/β-catenin signaling pathway. [J Cancer Res Clin Oncol. 2024]
MEX3A promotes colorectal cancer migration, invasion and EMT via regulating the Wnt/β-catenin signaling pathway.
Xu J, Chen S, Hao T, Liu G, Zhang K, Zhang C, He Y. J Cancer Res Clin Oncol. 2024 Jun 25; 150(6):319. Epub 2024 Jun 25.
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.

RefSeq alternative splicing
See 28 reference mRNA sequence splice variants for the LMNA gene.

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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Full text in PMC
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OMIM
OMIM records associated with Nucleotide sequence
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RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.
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Nucleotide