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Symbol
Name
ID

Lama2
laminin, alpha 2
MGI:99912

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties in infancy	Weak cry
Disease(s) Associated with LAMA2	Feeding difficulties in infancy	Weak cry
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

Availability

Mouse Genotype

Lama2^dy-2J/Lama2^dy-2J

Lama2^dy-6J/Lama2^dy-6J

Lama2^dy-7J/Lama2^dy-7J

Lama2^dy-8J/Lama2^dy-8J

Lama2^dy-Pas/Lama2^dy-Pas

Lama2^dy/Lama2^dy

Lama2^tm1Eeng/Lama2^tm1Eeng

Lama2^tm1Stk/Lama2^tm1Stk

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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