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Phenotypes Associated with This Genotype
Genotype
MGI:2660662
Allelic
Composition
Ccd/Ccd+
Genetic
Background
involves: 101 * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• partial or complete failure of ossification of cranial fontanelles
• partial or complete failure of ossification of clavicles
• partial or complete failure of ossification of symphysis pubis
• partial or complete failure of ossification of clavicles, symphysis pubis, and cranial fontanelles

craniofacial
• partial or complete failure of ossification of cranial fontanelles

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cleidocranial dysplasia DOID:13994 OMIM:119600
OMIM:216330
J:14006


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/19/2021
MGI 6.16
The Jackson Laboratory