Laminin subunit alpha-1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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

PDBOrtholog search: PDBe RCSB
AliasesLAMA1, LAMA, S-LAM-alpha, PTBHS, Laminin, alpha 1, laminin subunit alpha 1
Quick facts LAMA1, Available structures ...
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; OMA:LAMA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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
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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

Further reading

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