LAMA1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLAMA1, LAMA, S-LAM-alpha, PTBHS, Laminin, alpha 1, laminin subunit alpha 1
External IDsOMIM: 150320 MGI: 99892 HomoloGene: 21146 GeneCards: LAMA1
Orthologs
SpeciesHumanMouse
Entrez

284217

16772

Ensembl

ENSG00000101680

ENSMUSG00000032796

UniProt

P25391

P19137

RefSeq (mRNA)

NM_005559

NM_008480

RefSeq (protein)

NP_005550

NP_032506

Location (UCSC)Chr 18: 6.94 – 7.12 MbChr 17: 68 – 68.13 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Laminin subunit alpha-1 is a protein that in humans is encoded by the LAMA1 gene.[5][6]

Interactions

Laminin, alpha 1 has been shown to interact with FBLN2.[7][8]

Role in pathology

Mutations of the LAMA1 gene cause the Poretti–Boltshauser syndrome.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000101680 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000032796 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 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.
  6. "Entrez Gene: LAMA1 laminin, alpha 1".
  7. 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.
  8. 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.

Further reading

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