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Symbol
Name
ID

Lama2
laminin, alpha 2
MGI:99912

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Abnormality of the temporomandibular joint	Myopathic facies	Facial palsy	Macroglossia	Protruding tongue	Open mouth	Impaired mastication
Disease(s) Associated with LAMA2
congenital merosin-deficient muscular dystrophy 1A

Mouse Phenotypes		abnormal cranium morphology	abnormal bony labyrinth	increased cranium width
Availability	Mouse Genotype	abnormal cranium morphology	abnormal bony labyrinth	increased cranium width
	Lama2^dy-2J/Lama2^dy-2J
	Lama2^dy/Lama2^dy

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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