LAMA2 Chromosome 6

Laminin subunit alpha 2
1142 variants 1142 Health Risk

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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
RS1012171328 Health Risk Conflicting classifications of pathogenicity Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS1024374408 Health Risk Conflicting classifications of pathogenicity Myalgia, Elevated circulating creatine kinase concentration, Exercise-induced myalgia
RS1057523624 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1057524616 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1064795750 Health Risk Conflicting classifications of pathogenicity Muscular dystrophy, limb-girdle, autosomal recessive 23
RS111632017 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder, LAMA2-related muscular dystrophy
RS112388307 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related disorder, LAMA2-related muscular dystrophy
RS112637707 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS113022759 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Muscular dystrophy
RS115488979 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, LAMA2-related disorder
RS115650537 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS117116822 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS117422805 Health Risk Conflicting classifications of pathogenicity Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Intellectual disability
RS117884199 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, LAMA2-related disorder
RS118083923 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, Inborn genetic diseases
RS118147866 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS121913570 Health Risk Conflicting classifications of pathogenicity Merosin deficient congenital muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS121913573 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS121913574 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS1221715098 Health Risk Conflicting classifications of pathogenicity Merosin deficient congenital muscular dystrophy, LAMA2-related disorder, Muscular dystrophy
RS1256347636 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS1281520681 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS1293824666 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS1307580344 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Muscular dystrophy, limb-girdle
RS1334243603 Health Risk Conflicting classifications of pathogenicity Muscular dystrophy, limb-girdle, autosomal recessive 23
RS137962409 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS138024644 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS138162760 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Inborn genetic diseases
RS138303386 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, Inborn genetic diseases
RS138695453 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS138732723 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS139070796 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS139159258 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related disorder, LAMA2-related muscular dystrophy
RS139244736 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Inborn genetic diseases, LAMA2-related disorder
RS139351727 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS139455685 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS139586720 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS139739075 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS139824017 Health Risk Conflicting classifications of pathogenicity Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
RS139843107 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Muscular dystrophy
RS140178576 Health Risk Conflicting classifications of pathogenicity Muscular dystrophy, limb-girdle, autosomal recessive 23
RS140202046 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Muscular dystrophy
RS140483001 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS140604077 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Muscular dystrophy
RS140658201 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS141000358 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS141101234 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS141190803 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS141235562 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Muscular dystrophy
RS141340479 Health Risk Conflicting classifications of pathogenicity Merosin deficient congenital muscular dystrophy, Muscular dystrophy, limb-girdle
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