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Lama2dy-8J
Spontaneous Allele Detail
Nomenclature
Symbol: Lama2dy-8J
Name: laminin, alpha 2; dystrophia muscularis 8 Jackson
MGI ID: MGI:3848931
Gene: Lama2  Location: Chr10:26981285-27617191 bp, - strand  Genetic Position: Chr10, 14.23 cM, cytoband A4-B1
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    A non-complementation test with Lama2 proved that this mutation is an allele of Lama2.
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 2 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Lama2 Mutation:  106 strains or lines available
References
Original:  J:149729 Harris B, et al., Lama2: A new remutation to dystrophia muscularis. MGI Direct Data Submission. 2009;
All:  1 reference(s)

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
02/23/2021
MGI 6.16
The Jackson Laboratory