About   Help   FAQ
Ccd
Radiation induced Allele Detail
Nomenclature
Symbol: Ccd
Name: cleidocranial dysplasia
MGI ID: MGI:1861187
Synonyms: 320
Gene: Ccd  Location: unknown  Genetic Position: Chr17, Syntenic
Mutation
origin
Strain of Origin:  101
Mutation
description
Allele Type:    Radiation induced
Mutation:    Intergenic deletion
 
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Ccd Mutation:  0 strains or lines available
Notes
Induced by gamma irradiation in a 101 strain male. Heterozygotes show striking homology to cleidocranial dysplasia, a skeletal disorder in man. The mutation is fully penetrant in heterozygotes. It causes partial or complete failure of ossification of clavicles, symphysis pubis, and cranial fontanelles. This mutation is lethal in homozygotes (J:14006).

References
Original:  J:14006 Selby P, et al., Cleidocranial dysplasia, Ccd. Mouse News Lett. 1985;72:123
All:  6 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
04/08/2014
MGI 5.17
The Jackson Laboratory