|
Symbol Name ID |
Cplane1
ciliogenesis and planar polarity effector 1 MGI:1920942 |
| Darker colors indicate more annotations |
| Human Phenotypes | Oculomotor apraxia |
Polymicrogyria |
Aplasia/Hypoplasia of the corpus callosum |
Agenesis of corpus callosum |
Porencephalic cyst |
Hypothalamic hamartoma |
Arrhinencephaly |
Cerebellar vermis hypoplasia |
Molar tooth sign on MRI |
Arachnoid cyst |
Occipital meningocele |
Abnormality of neuronal migration |
Periventricular nodular heterotopia |
Hypoplasia of olfactory tract |
Ataxia |
Tremor |
Intellectual disability |
Gait disturbance |
Global developmental delay |
Seizure |
| Disease(s) Associated with CPLANE1 | ||||||||||||||||||||
| Joubert syndrome 17 | ||||||||||||||||||||
| Joubert syndrome with orofaciodigital defect |
| Mouse Phenotypes | decreased brain size |
abnormal cerebellum morphology |
|
| Availability | Mouse Genotype | ||
| Cplane1b2b012Clo/Cplane1b2b012Clo | |||
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 04/23/2024 MGI 6.23 |
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