Ighmbp2^nmd
Spontaneous Allele Detail

Summary

• Symbol: Ighmbp2^nmd
• Name: immunoglobulin mu DNA binding protein 2; neuromuscular degeneration
• MGI ID: MGI:1857647
• Synonyms: nmd^J
• Gene: Ighmbp2 Location: Chr19:3309076-3333011 bp, - strand Genetic Position: Chr19, 3.03 cM
• Alliance: Ighmbp2^nmd page

Mutation origin

• Strain of Origin: CBA/J

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• Mutation details: A 3 bp deletion in exon 8 resulted in a deletion of a conserved leucine residue in the encoded protein. (J:51890)
• Inheritance: Recessive

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

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 Ighmbp2 Mutation: 46 strains or lines available

Notes

Extinct. Genomic DNA has been preserved.

References

• Original: J:23584 Cook SA, et al., Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration. Mamm Genome. 1995 Mar;6(3):187-91
• All: 6 reference(s)