The LMNA gene homepage

General information
Gene symbol LMNA
Gene name lamin A/C
Chromosome 1
Chromosomal band q22
Imprinted -
Genomic reference NG_008692.1
Transcript reference NM_170707.2
Associated with diseases WD
Citation reference(s) Pan M et al, 2011
Zhang T et al, 2010
Refseq URL Coding DNA reference sequence
Curators (0) -
Total number of public variants reported 475
Unique public DNA variants reported 229
Individuals with public variants 0
Hidden variants -
Notes The nuclear lamina consists of a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. [provided by RefSeq, Apr 2012]
Also known as: FPL; IDC; LFP; CDDC; EMD2; FPLD; HGPS; LDP1; LMN1; LMNC; PRO1; CDCD1; CMD1A; FPLD2; LMNL1; CMT2B1; LGMD1B
Date created April 21, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL http://www.genomed.org/lovd3/genes/LMNA
External URL Inherited Peripheral Neuropathies Mutation Database
Intermediate Filament Details
Leiden Muscular Dystrophy pages
The UMD-LMNA mutations database
HGNC 6636
Entrez Gene 4000
PubMed articles LMNA
OMIM - Gene 150330
OMIM - Diseases WD (wilson disease)
HGMD LMNA
GeneCards LMNA
GeneTests LMNA


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000079 1 lamin A/C NM_170707.2 - 475


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