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Symbol
Name
ID
Lama2
laminin, alpha 2
MGI:99912
Phenotype annotations related to skeleton
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
Availability Mouse Genotype
Lama2dy-2J/Lama2dy-2J
Lama2dy-6J/Lama2dy-6J
Lama2dy-Pas/Lama2dy-Pas
Lama2dy/Lama2dy

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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory