This family has 11 members: 1 Caenorhabditis elegans, 1 Danio rerio, 1 Drosophila melanogaster, 2 Gallus gallus, 2 Homo sapiens, 2 Mus musculus, 2 Rattus norvegicus.
Interactive Java Applets: Notung Tree Analysis · Jalview Alignment
| Organism | Protein (Synonyms) | Description | AmiGO |
|---|---|---|---|
| C. elegans | UniProtKB:O45614 · WB:WBGene00002248 (lam-3 · T22A3.8) |  | |
| D. rerio | UniProtKB:Q45H72 · ZFIN:ZDB-GENE-060118-1 (lama1) | laminin, alpha 1 | |
| D. melanogaster | UniProtKB:Q8IP51 · FB:FBgn0004002 (l(2)09437 · BG:DS03792.1 · A1 · wb · l34Fb · CK02229 · laminin · CG15288 · l(2)br1 · DLAM · CT35236 · l(2)34Fb · LM-A/alpha2 · BEST:CK02229 · lamininW) | alpha laminin · wing blistered · lethal 1 in the black-reduced region · Laminin alpha1,2 · D-laminin alpha2 · laminin alpha1,2 · wing blister · lethal group A1 | |
| G. gallus | NCBI:XP_419746 · ENTREZ:421709 | ||
| G. gallus | ENTREZ:374016 · NCBI:XP_419139 | ||
| H. sapiens | ENSEMBL:ENSG00000101680 · UniProtKB:P25391 (IPI00375294 · P25391 · LAMA · LAMA1 · LAMA1_HUMAN) | Laminin subunit alpha-1 | |
| H. sapiens | ENSEMBL:ENSG00000196569 · UniProtKB:P24043 (LAMA2_HUMAN · LAMA2 · P24043 · LAMM · IPI00844276) | Laminin subunit alpha-2 | |
| M. musculus | UniProtKB:P19137 · MGI:MGI:99892 (Lama · Lama1) | laminin, alpha 1 | |
| M. musculus | UniProtKB:Q60675 · MGI:MGI:99912 (merosin · mer · Lama2) | laminin, alpha 2 | |
| R. norvegicus | NCBI:XP_001062273 · RGD:1308889 (Lama2) | laminin, alpha 2 | |
| R. norvegicus | NCBI:NP_001101707 · RGD:1307207 (Lama1) | laminin, alpha 1 | |
No functional conservation results.
| Description | Suffix |
|---|---|
| Sequences in this family | .fasta |
| mafft aligned Fasta file | .afasta |
| phyml newick file | .newick |
| Notung rooted & rearranged newick file | .newick.rooting.0.rearrange.0 |
| Notung Homolog Table | .newick.rooting.0.rearrange.0.homologs.csv |
| OMIM (1) | |
|---|---|
| ENSEMBL:ENSG00000196569 · UniProtKB:P24043 | #607855 MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A;;MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENTMUSCULAR DYSTROPHY, CONGENITAL, DUE TO PARTIAL LAMA2 DEFICIENCY, INCLUDED |