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LAMA3

laminin subunit alpha 3
3 disorders 2 untyped 1 no genetic record 18q11.2 gene with protein product
HGNC:6483MonarchNCBI Gene 3909ENSG00000053747UniProt Q16787OMIM 600805

Previous symbols: LAMNA. Aliases: nicein-150kDa, kalinin-165kDa, BM600-150kDa, epiligrin.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Epidermolysis Bullosa untyped
Causative
mechanism: Basement Membrane Zone Structural Disruption
Junctional Epidermolysis Bullosa untyped
Causative
mechanism: Laminin-332 Deficiency
subtype: JEB Intermediate (Non-Herlitz / Generalized Atrophic Benign EB); JEB Severe (Herlitz); LOC Syndrome
Mucous Membrane Pemphigoid no genetic record
mechanism: Anti-Basement Membrane Zone Autoantibody Production
subtype: Anti-laminin 332 MMP
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.