Ccd Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ccd
cleidocranial dysplasia
MGI:88291

22 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ccd/Ccd⁺ B10Rl.101-Ccd	abnormal axial skeleton morphology	J:16170
	abnormal clavicle morphology	J:16170
	abnormal cranium morphology	J:16170
	abnormal humerus morphology	J:16170
	abnormal interparietal bone morphology	J:16170
	abnormal ischium morphology	J:16170
	abnormal neurocranium morphology	J:16170
	abnormal orbit morphology	J:16170
	abnormal pectoral girdle bone morphology	J:16170
	abnormal pelvic girdle bone morphology	J:16170
	abnormal pubis morphology	J:16170
	abnormal scapula morphology	J:16170
	abnormal temporal bone squamous part morphology	J:16170
	abnormal vertebrae morphology	J:16170
	abnormal xiphoid process morphology	J:16170
	absent deltoid tuberosity	J:16170
	absent nasal bone	J:16170
Ccd/Ccd⁺ involves: 101 * C3H	abnormal clavicle morphology	J:14006
	abnormal fontanelle morphology	J:14006
	abnormal pubic symphysis morphology	J:14006
	failure of bone ossification	J:14006
Ccd/Ccd involves: 101 * C3H	embryonic lethality, complete penetrance	J:16170
Ccd/Ccd involves: 101 * C3H	preweaning lethality, complete penetrance	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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