|
Symbol Name ID |
Myt1l
myelin transcription factor 1-like MGI:1100511 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Hydrocephalus |
Thin corpus callosum |
Cerebral atrophy |
Delayed speech and language development |
Autistic behavior |
Polyphagia |
Aggressive behavior |
Self-mutilation |
Intellectual disability |
Global developmental delay |
Delayed gross motor development |
Delayed ability to walk |
Focal impaired awareness seizure |
Generalized non-motor (absence) seizure |
| Disease(s) Associated with MYT1L | ||||||||||||||
| autosomal dominant intellectual developmental disorder 39 |
| Mouse Phenotypes | nervous system phenotype |
decreased neuronal precursor proliferation |
abnormal brain development |
decreased brain weight |
decreased brain size |
abnormal brain white matter morphology |
decreased corpus callosum size |
abnormal dendritic mushroom spine morphology |
increased dendritic spine density |
abnormal dendritic stubby spine morphology |
abnormal dendritic thin spine morphology |
abnormal neuron physiology |
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| Availability | Mouse Genotype | ||||||||||||
| Myt1lem1Mwer/Myt1lem1Mwer | * | ||||||||||||
| Myt1lem1Jdd/Myt1l+ | |||||||||||||
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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