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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cdon
cell adhesion molecule-related/down-regulated by oncogenes
MGI:1926387
39 phenotypes from 4 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cdontm1Aok/Cdontm1Aok
involves: 129P2/OlaHsd * CD-1
normal nervous system phenotype J:115577
Cdontm1b(EUCOMM)Hmgu/Cdontm1b(EUCOMM)Hmgu
C57BL/6N-Cdontm1b(EUCOMM)Hmgu/Orl
preweaning lethality, incomplete penetrance J:211773
Cdontm1Rsk/Cdontm1Rsk
B6.129-Cdontm1Rsk
abnormal blood vessel morphology J:109070
abnormal brain ventricle morphology J:109070
abnormal cerebral cortex morphology J:109070
abnormal forebrain morphology J:109070
abnormal neuronal precursor proliferation J:109070
absent lamina terminalis J:109070
domed cranium J:109070
enlarged lateral ventricles J:109070
hemorrhage J:109070
holoprosencephaly J:109070
hydrocephaly J:109070
perinatal lethality, incomplete penetrance J:109070
premature death J:109070
thin cerebral cortex J:109070
weakness J:109070
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac
abnormal craniofacial development J:171767
abnormal maxilla morphology J:171767
abnormal maxillary shelf morphology J:171767
abnormal palate development J:171767
abnormal premaxilla morphology J:171767
absent maxillary shelf J:171767
basisphenoid bone foramen J:171767
decreased maxillary shelf size J:171767
small basisphenoid bone J:171767
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * C57BL/6
abnormal craniofacial morphology J:82221
abnormal nose morphology J:82221
abnormal philtrum morphology J:82221
abnormal premaxilla morphology J:82221
abnormal upper incisor morphology J:82221
absent nasal septum cartilage J:82221
absent primary palate J:82221
absent upper incisors J:82221
basisphenoid bone foramen J:82221
decreased body size J:82221
holoprosencephaly J:82221
nasal septum cartilage hypoplasia J:82221
neonatal lethality, incomplete penetrance J:82221
piriform aperture stenosis J:82221
postnatal lethality, incomplete penetrance J:82221
small basisphenoid bone J:82221
small nasal septum J:82221
Cdontm2Rsk/Cdontm2Rsk
B6.129-Cdontm2Rsk
abnormal blood vessel morphology J:109070
abnormal brain ventricle morphology J:109070
abnormal cerebral cortex morphology J:109070
abnormal forebrain morphology J:109070
abnormal neuronal precursor proliferation J:109070
absent lamina terminalis J:109070
domed cranium J:109070
enlarged lateral ventricles J:109070
hemorrhage J:109070
holoprosencephaly J:109070
hydrocephaly J:109070
perinatal lethality, incomplete penetrance J:109070
premature death J:109070
thin cerebral cortex J:109070
weakness J:109070
Cdontm2Rsk/Cdontm2Rsk
involves: 129/Sv * C57BL/6
abnormal craniofacial morphology J:82221
abnormal nose morphology J:82221
abnormal philtrum morphology J:82221
abnormal premaxilla morphology J:82221
abnormal upper incisor morphology J:82221
absent nasal septum cartilage J:82221
absent primary palate J:82221
absent upper incisors J:82221
basisphenoid bone foramen J:82221
decreased body size J:82221
holoprosencephaly J:82221
nasal septum cartilage hypoplasia J:82221
neonatal lethality, incomplete penetrance J:82221
piriform aperture stenosis J:82221
postnatal lethality, incomplete penetrance J:82221
small basisphenoid bone J:82221
small nasal septum J:82221

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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
04/30/2024
MGI 6.23
The Jackson Laboratory