About   Help   FAQ
Cm
Radiation induced Allele Detail
Nomenclature
Symbol: Cm
Name: coloboma deletion region; coloboma
MGI ID: MGI:1861106
Gene: Cm  Location: unknown  Genetic Position: Chr2, Syntenic
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
Inheritance:    Semidominant
Phenotypes
Loading...
View phenotypes for all genotypes (concatenated display).
Disease models
Loading...
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/09/2014
MGI 5.19
The Jackson Laboratory