Symbol Name ID |
Lama2
laminin, alpha 2 MGI:99912 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Weak cry |
Disease(s) Associated with LAMA2 | ||
congenital merosin-deficient muscular dystrophy 1A |
Mouse Phenotypes | decreased aggression |
abnormal motor capabilities/coordination/movement |
abnormal reflex |
limb grasping |
opisthotonus |
abnormal motor coordination/balance |
ataxia |
abnormal gait |
decreased locomotor activity |
hindlimb paralysis |
paresis |
hindlimb paresis |
abnormal sexual interaction |
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Availability | Mouse Genotype | |||||||||||||
Lama2dy-2J/Lama2dy-2J | ||||||||||||||
Lama2dy-6J/Lama2dy-6J | ||||||||||||||
Lama2dy-7J/Lama2dy-7J | ||||||||||||||
Lama2dy-8J/Lama2dy-8J | ||||||||||||||
Lama2dy-Pas/Lama2dy-Pas | ||||||||||||||
Lama2dy/Lama2dy | ||||||||||||||
Lama2tm1Eeng/Lama2tm1Eeng | ||||||||||||||
Lama2tm1Stk/Lama2tm1Stk |
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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