LAMA2
This page contains an overview of the genetic variation in the LAMA2 gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:
LAMA2 gene and transcript details
Gene Name
laminin, alpha 2
Gene Links
Ensembl: ENSG00000196569 -
Locus Reference Genomic: LRG_409
Genomic Location
Chromosome 6 : 129,204,391 - 129,837,492 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (9366 bases) | Protein (3122 aa) |
|---|---|---|
 |
ENST00000421865 | ENSP00000400365 |
 |
LRG_409t1 | LRG_409p1 |
 |
NM_000426.3 | |
 |
P24043 |
Summary of LAMA2 in Cardiomyopathies
LAMA2 variants in ExAC
Details of the protein-altering LAMA2 variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.
| Total Variants | Combined frequency of rare variants | |
|---|---|---|
| All Variants | 1388 | 0.02138 |
| Truncating | 95 | 0.00139 |
| Missense | 1153 | 0.01834 |
| Inframe | 9 | 0.00012 |
| Splice Site | 131 | 0.00152 |