| GENE NAME | LAMA2 |
| CHROMOSOME | 6 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000196569 |
| UNIPROT ACCESSION NUMBER | P24043 |
| GO MOLECULAR FUNCTION | ['structural molecule activity', 'signaling receptor binding', 'extracellular matrix structural constituent'] |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa04151; hsa04510; hsa04512; hsa05145; hsa05146; hsa05165; hsa05200; hsa05222; hsa05410; hsa05412; hsa05414; hsa05416; R-HSA-1266738; R-HSA-1474244; R-HSA-162582; R-HSA-3000157; R-HSA-3000171; R-HSA-3000178; R-HSA-6806834; R-HSA-8874081; R-HSA-8875878; R-HSA-9006934; R-HSA-9619665; R-HSA-9675108 |
| 2 combinations linked to LAMA2 | OLI1697; OLI982 |
| 2 variants linked to LAMA2 | LAMA2:c.379A>G, p.Thr127Ala; LAMA2:c.4879C>T, p.Arg1627Trp |
| 2 diseases linked to LAMA2 | Schizophrenia; Congenital nephrotic syndrome |