ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

Gene Report

Basic Info
Approved Symbol LAMA2
Previous Symbol LAMM
Approved Name laminin, alpha 2
Name Alias "merosin", "congenital muscular dystrophy"
Location 6q22-q23
Position chr6:129204342-129837714, 1
External Links HGNC: 6482
Entrez Gene: 3908
Ensembl: ENSG00000196569
UCSC: uc003qbn.3
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source Mapped by CNV; Mapped by significant region

Gene related studies (count: 0)

Gene related SNPs (count: 0)

Gene related CNVs (count: 1)

Gene related other variant (count: 0)

Gene related regions (count: 1)

Gene related GO terms (count: 14)

GO terms by PBA (with statistical significance of FDR<0.05) (count: 0)

GO terms by database search (count: 14)

Gene related KEGG pathways (count: 4)

Genes shared at least 5 GO terms with LAMA2 (count: 3)

Genes shared at least 2 KEGG pathways with LAMA2 (count: 15)

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Region: chr6:129204342..129837714 View in gBrowse
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