|
Symbol Name ID |
Tubg1
tubulin, gamma 1 MGI:101834 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Dysphagia |
Spastic tetraplegia |
Agyria |
Pachygyria |
Subcortical band heterotopia |
Thick corpus callosum |
Thin corpus callosum |
Reduced tendon reflexes |
Hyporeflexia |
Global developmental delay |
Seizure |
Infantile spasms |
| Disease(s) Associated with TUBG1 | |||||||||||||
| complex cortical dysplasia with other brain malformations 4 | |||||||||||||
| inclusion body myositis |
| Mouse Phenotypes | nervous system phenotype |
increased susceptibility to pharmacologically induced seizures |
decreased brain size |
abnormal brain white matter morphology |
abnormal anterior commissure morphology |
abnormal hippocampus CA1 region morphology |
decreased cerebral cortex total cell area |
decreased premotor cortex size |
abnormal stratification in cerebral cortex |
thin cerebral cortex |
small cerebellum |
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| Availability | Mouse Genotype | |||||||||||
| Tubg1tm1.1Ics/Tubg1+ | * | |||||||||||
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 05/21/2024 MGI 6.23 |
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