|
Symbol Name ID |
Micu1
mitochondrial calcium uptake 1 MGI:2384909 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Increased CSF protein concentration |
Progressive extrapyramidal muscular rigidity |
Difficulty walking |
Easy fatigability |
Frequent falls |
Peripheral axonal neuropathy |
Perisylvian polymicrogyria |
Abnormal basal ganglia MRI signal intensity |
Hypoplastic anterior limbs of the internal capsule |
Encephalomalacia |
Cerebellar dysplasia |
Ataxia |
Clumsiness |
Abnormality of extrapyramidal motor function |
Progressive extrapyramidal movement disorder |
Choreoathetosis |
Chorea |
Clonus |
Involuntary movements |
Tremor |
Resting tremor |
Delayed speech and language development |
Hyperactivity |
Orofacial dyskinesia |
Dystonia |
Global developmental delay |
Motor delay |
Specific learning disability |
Seizure |
Status epilepticus |
| Disease(s) Associated with MICU1 | |||||||||||||||||||||||||||||||
| myopathy with extrapyramidal signs |
| Mouse Phenotypes | abnormal brain development |
abnormal cerebellum development |
abnormal Purkinje cell dendrite morphology |
|
| Availability | Mouse Genotype | |||
| Micu1em#Fink/Micu1em#Fink | ||||
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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