Symbol Name ID |
Lama2
laminin, alpha 2 MGI:99912 |
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 |
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Availability | Mouse Genotype | |||
Lama2dy-2J/Lama2dy-2J | ||||
Lama2dy/Lama2dy |
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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last database update 09/03/2024 MGI 6.24 |
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