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Lama2dy
Spontaneous Allele Detail
Nomenclature
Symbol: Lama2dy
Name: laminin, alpha 2; dystrophia muscularis
MGI ID: MGI:1856026
Synonyms: dy
Gene: Lama2  Location: Chr10:26981288-27616942 bp, - strand  Genetic Position: Chr10, 14.23 cM, cytoband A4-B1
Lama2dy/Lama2dy and control

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  129P1/Re
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation details
Inheritance:    Recessive
Phenotypes
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Disease models
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Expression
In Mice Carrying this Mutation: 9 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Lama2 Mutation:  7 strains or lines available
Notes
This mutation arose spontaneously in the 129/Re inbred strain at The Jackson Laboratory in 1951.

References
Original:  J:13125 Michelson AM, et al., Dystrophia muscularis: a hereditary primary myopathy in the house mouse. Proc Natl Acad Sci U S A. 1955 Dec 15;41(12):1079-1084
All:  64 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/23/2014
MGI 5.19
The Jackson Laboratory