Phenotypes Associated with This Genotype

Genotype
MGI:2660662

• Allelic Composition: Ccd/Ccd⁺
• Genetic Background: involves: 101 * C3H

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

skeleton

abnormal fontanelle morphology ( J:14006 )

• partial or complete failure of ossification of cranial fontanelles

abnormal clavicle morphology ( J:14006 )

• partial or complete failure of ossification of clavicles

abnormal pubic symphysis morphology ( J:14006 )

• partial or complete failure of ossification of symphysis pubis

failure of bone ossification ( J:14006 )

• partial or complete failure of ossification of clavicles, symphysis pubis, and cranial fontanelles

craniofacial

abnormal fontanelle morphology ( J:14006 )

• 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