LAMA2 Chromosome 6

Laminin subunit alpha 2
1142 variants 1142 Health Risk

Upload your DNA to see your personal genotypes for variants in LAMA2.

What This Gene Does
Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Laminin subunits
Locus Type
gene with protein product
Location
6q22.33
Ensembl
ENSG00000196569
Associated Conditions (35)
Merosin deficient congenital muscular dystrophy
LAMA2-related muscular dystrophy
Myalgia
Elevated circulating creatine kinase concentration
Exercise-induced myalgia
Muscular dystrophy
limb-girdle
autosomal recessive 23
Congenital muscular dystrophy due to partial LAMA2 deficiency
LAMA2-related disorder
Intellectual disability
Inborn genetic diseases
Malignant tumor of esophagus
Primary dilated cardiomyopathy
Malignant tumor of urinary bladder
Familial cancer of breast
Ovarian cancer
Cervical cancer
Rare genetic intellectual disability
See cases
+15 more conditions
Key Variants
RS1012171328
Conflicting classifications of pathogenicity
Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
Health Risk
RS1024374408
Conflicting classifications of pathogenicity
Myalgia, Elevated circulating creatine kinase concentration, Exercise-induced myalgia
Health Risk
RS1057523624
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
Health Risk
RS1057524616
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
Health Risk
RS1064795750
Conflicting classifications of pathogenicity
Muscular dystrophy, limb-girdle, autosomal recessive 23
Health Risk
RS111632017
Conflicting classifications of pathogenicity
Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder, LAMA2-related muscular dystrophy
Health Risk
RS112388307
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, LAMA2-related disorder, LAMA2-related muscular dystrophy
Health Risk
RS112637707
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
Health Risk
RS113022759
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Muscular dystrophy
Health Risk
RS115488979
Conflicting classifications of pathogenicity
Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, LAMA2-related disorder
Health Risk
RS115650537
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
Health Risk
RS117116822
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
Health Risk
All Variants (1142)
RSID Category Clinical Significance Conditions
RS1131691660 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1165626901 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1187391940 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1190231274 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1196380787 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1207051921 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1211739649 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1217170426 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1217989194 Health Risk Likely pathogenic Abnormality of the musculature, Abnormality of the musculature
RS1222759165 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1223081122 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1226441435 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1231027193 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1231305572 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1244029486 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1247084547 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1256470015 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1278823424 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1301666663 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1330890210 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1370654793 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1377818460 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1383756739 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1404492484 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1415944134 Health Risk Likely pathogenic Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1423432874 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS143215851 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1433459701 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1436470033 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1441766008 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1443920683 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1462522184 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS1463264889 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS148433965 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1490493934 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554217476 Health Risk Likely pathogenic
RS1554226186 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554234051 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554256965 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554290316 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554299897 Health Risk Likely pathogenic
RS1554301637 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554303937 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554310169 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554310242 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1554319117 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Muscular dystrophy
RS1554321125 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1562273395 Health Risk Likely pathogenic Muscular dystrophy, limb-girdle, autosomal recessive 23
RS1562281922 Health Risk Likely pathogenic LAMA2-related muscular dystrophy, Muscular dystrophy, limb-girdle
RS1562449164 Health Risk Likely pathogenic Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
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