Symbol Name ID |
Lama2
laminin, alpha 2 MGI:99912 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the temporomandibular joint |
Scapular winging |
Flexion contracture |
Intercostal muscle weakness |
Hyperlordosis |
Kyphoscoliosis |
Scoliosis |
Disease(s) Associated with LAMA2 | |||||||
congenital merosin-deficient muscular dystrophy 1A | |||||||
muscular dystrophy |
Mouse Phenotypes | abnormal cranium morphology |
abnormal bony labyrinth |
increased cranium width |
kyphosis |
kyphoscoliosis |
scoliosis |
abnormal joint morphology |
joint contracture |
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Availability | Mouse Genotype | ||||||||
Lama2dy-2J/Lama2dy-2J | |||||||||
Lama2dy-6J/Lama2dy-6J | |||||||||
Lama2dy-Pas/Lama2dy-Pas | |||||||||
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 03/19/2024 MGI 6.23 |
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