Symbol Name ID |
Myo5a
myosin VA MGI:105976 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Cerebral calcification |
Ataxia |
Intellectual disability |
Abnormality of movement |
Global developmental delay |
Seizure |
Disease(s) Associated with MYO5A | ||||||
Griscelli syndrome type 1 |
Mouse Phenotypes | nervous system phenotype |
seizures |
clonic seizures |
myoclonus |
abnormal cerebellum morphology |
abnormal Purkinje cell dendrite morphology |
reduced long-term depression |
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Availability | Mouse Genotype | |||||||
Myo5ad-15H/Myo5ad-15H | ||||||||
Myo5ad-l32J/Myo5ad-l32J | ||||||||
Myo5ad-l/Myo5ad-l | ||||||||
Myo5ad-n2Btlr/Myo5ad-n2Btlr | ||||||||
Myo5ad-n/Myo5ad-n | ||||||||
Myo5ad-nBtlr/Myo5ad-nBtlr | * |
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 05/14/2024 MGI 6.23 |
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