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Symbol Name ID |
Rogdi
rogdi homolog MGI:1913299 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Spasticity |
Hydrocephalus |
Ventriculomegaly |
Cerebral atrophy |
Cerebellar hypoplasia |
Ataxia |
EEG abnormality |
Hypsarrhythmia |
Delayed speech and language development |
Mental deterioration |
Dementia |
Intellectual disability |
Intellectual disability, severe |
Epileptic encephalopathy |
Developmental regression |
Global developmental delay |
Delayed ability to walk |
Seizure |
Bilateral tonic-clonic seizure |
Focal-onset seizure |
Myoclonic seizure |
| Disease(s) Associated with ROGDI | ||||||||||||||||||||||
| Kohlschutter-Tonz syndrome |
| Mouse Phenotypes | increased susceptibility to pharmacologically induced seizures |
abnormal cerebellum external granule cell layer morphology |
abnormal dentate gyrus morphology |
thin hippocampus stratum oriens |
abnormal lobule simplex morphology |
abnormal paramedian lobule morphology |
thin cerebellar granule layer |
thin cerebellar molecular layer |
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| Availability | Mouse Genotype | ||||||||
| Rogditm1.2Ics/Rogditm1.2Ics | |||||||||
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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