LAMA2 laminin subunit alpha 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 3908)
Symbol: LAMA2
Full name: laminin subunit alpha 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: LAMM; MDC1A
Summary: Laminin, an extracellular 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. [provided by RefSeq, Jul 2008]
Expression: Biased expression in placenta (RPKM 30.7), ovary (RPKM 13.2) and 11 other tissues
Orthologs: mouse
Gene size: 633429bp
Exon count: 65