Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:3908
  • Symbol:LAMA2
  • Description:laminin subunit alpha 2

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Disease_Term Source Rank Other Values
Muscular dystrophy, congenital, due to partial LAMA2 deficiency, 607855 (3) OMIM high
  • Genome region :6q22.33
  • OMIM_ID :156225OMIM gene ID
  • OMIM_ID :607855OMIM phenotype ID
Muscular dystrophy, congenital merosin-deficient, 607855 (3) OMIM high
  • Genome region :6q22.33
  • OMIM_ID :156225OMIM gene ID
  • OMIM_ID :607855OMIM phenotype ID
Refractive error GWAS high
Body mass index GWAS high
Myopia GWAS high
Spherical equivalent (joint main effects and education interaction) GWAS high
Hyperopia GWAS high
Night sleep phenotypes GWAS high
Amyotrophic lateral sclerosis (sporadic) GWAS high
Periodontal disease-related phenotypes GWAS high
Axial length GWAS high