Lama2^dy-7J
Chemically induced Allele Detail

Summary

• Symbol: Lama2^dy-7J
• Name: laminin, alpha 2; dystrophia muscularis 7, Jackson
• MGI ID: MGI:3581452
• Synonyms: Lama2^nmf417, neuroscience mutagenesis facility, 417, nmf417, NMF417
• Gene: Lama2 Location: Chr10:26857281-27493021 bp, - strand Genetic Position: Chr10, 14.23 cM, cytoband A4-B1
• Alliance: Lama2^dy-7J page

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Mutation details: This mutation was shown by complementation analysis versus the original, dystrophia muscularis mutation to be an allele of Lama2. The molecular lesion is a single base change from T to C at the first position of codon 79, which converts Cys79 to Arg. (J:134367)
• Inheritance: Recessive

Disease models

Expression

In Structures Affected by this Mutation:

3 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 1 strain available Cell Lines: 0 lines available
• Carrying any Lama2 Mutation: 177 strains or lines available

References

• Original: J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003
• All: 2 reference(s)