Gene: LAMA2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 Biomarker disease CTD_human
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. 7550355 1995
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 Biomarker disease GENOMICS_ENGLAND Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. 7550355 1995
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. 7550355 1995
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE Merosin-deficient congenital muscular dystrophy (CMD) is caused by mutations in the laminin alpha 2 chain gene. 9027848 1996
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain. 9185180 1997
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis. 9185182 1997
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis. 9185182 1997
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 Biomarker disease MGD Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy. 9326364 1997
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE This study provides valuable methods for determining the molecular defects in LAMA2 causing merosin deficient congenital muscular dystrophy. 9541105 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. 9541105 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 CausalMutation disease CLINVAR PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. 9541105 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients. 9674786 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 Biomarker disease MGD Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models. 9710454 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE These data confirm that mutations of the LAMA2 gene that do not completely disrupt the production of the protein can give rise to phenotypes considerably milder than classical merosin-deficient congenital muscular dystrophy. 9829280 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins. 10022829 1999
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophy. 10611118 2000
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 Biomarker disease MGD Activation of the lama2 gene in muscle regeneration: abortive regeneration in laminin alpha2-deficiency. 10616210 1999
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin. 10619025 1999
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Novel compound heterozygous laminina2-chain gene (LAMA2) mutations in congenital muscular dystrophy. Mutations in brief no. 159. Online. 10694916 1998
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease CLINVAR Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin. 10747011 2000
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease BEFREE Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci. 11053680 2000
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 CausalMutation disease CLINVAR Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping. 11287370 2001
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 Biomarker disease GENOMICS_ENGLAND Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study. 11591858 2001
Entrez Id: 3908
Gene Symbol: LAMA2
LAMA2 		1.000 GeneticVariation disease UNIPROT Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study. 11591858 2001