Cm
Radiation induced Allele Detail

Summary

• Symbol: Cm
• Name: coloboma deletion region; coloboma
• MGI ID: MGI:1861106
• Gene: Cm Location: unknown Genetic Position: Chr2, Syntenic
• Alliance: Cm page

Inner ear defects in Cm/+ mice

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

Mutation origin

• Strain of Origin: (C3H/HeH x 101/H)F1

Mutation description

• Allele Type: Radiation induced
• Mutation: Intergenic deletion
• Cm involves 29 genes/genome features (Hao1, Tmx4, Gm14037 ...) View all
• Mutation details: The deletion map of the Cm locus includes Snap25, Plcb, and some or all of Jag1, and numerous other DNA markers. (J:18309, J:54907)
• Inheritance: Semidominant

Disease models

Expression

In Structures Affected by this Mutation:

7 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 Cm Mutation: 1 strain or line available

Notes

This allele represents a deletion including Snap25, Plcb1

References

• Original: J:13451 Searle AG, Coloboma, Cm. Mouse News Lett. 1966;35:27
• All: 21 reference(s)