Laminin subunit alpha-2

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

Laminin subunit alpha-2 is a protein that in humans is encoded by the LAMA2 gene.[5][6][7]

PDBOrtholog search: PDBe RCSB
AliasesLAMA2, LAMM, Laminin, alpha 2, laminin subunit alpha 2, MDC1A
Quick facts LAMA2, Available structures ...
LAMA2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesLAMA2, LAMM, Laminin, alpha 2, laminin subunit alpha 2, MDC1A
External IDsOMIM: 156225; MGI: 99912; HomoloGene: 37306; GeneCards: LAMA2; OMA:LAMA2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000426
NM_001079823

NM_008481

RefSeq (protein)

NP_000417
NP_001073291

NP_032507

Location (UCSC)Chr 6: 128.88 – 129.52 MbChr 10: 26.86 – 27.5 Mb
PubMed search[3][4]
Wikidata
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Function

Laminin, an extracellular matrix protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene.[7]

References

Further reading

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