Protein-coding gene in the species Homo sapiens
Laminin subunit alpha-1 is a protein that in humans is encoded by the LAMA1 gene .[ 5] [ 6]
Laminin, alpha 1 has been shown to interact with FBLN2 .[ 7] [ 8]
Mutations of the LAMA1 gene cause the Poretti–Boltshauser syndrome .
^ a b c GRCh38: Ensembl release 89: ENSG00000101680 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032796 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Nagayoshi T, Mattei MG, Passage E, Knowlton R, Chu ML, Uitto J (January 1990). "Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3". Genomics . 5 (4): 932–5. doi :10.1016/0888-7543(89)90136-5 . PMID 2591971 .
^ "Entrez Gene: LAMA1 laminin, alpha 1" .
^ Utani A, Nomizu M, Yamada Y (January 1997). "Fibulin-2 binds to the short arms of laminin-5 and laminin-1 via conserved amino acid sequences" . J. Biol. Chem . 272 (5): 2814–20. doi :10.1074/jbc.272.5.2814 . ISSN 0021-9258 . PMID 9006922 . S2CID 24800195 .
^ Talts JF, Sasaki T, Miosge N, Göhring W, Mann K, Mayne R, Timpl R (November 2000). "Structural and functional analysis of the recombinant G domain of the laminin alpha4 chain and its proteolytic processing in tissues" . J. Biol. Chem . 275 (45): 35192–9. doi :10.1074/jbc.M003261200 . ISSN 0021-9258 . PMID 10934193 . S2CID 36521395 .
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