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Symbol Name ID |
Mapt
microtubule-associated protein tau MGI:97180 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of eye movement |
Supranuclear gaze palsy |
Vertical supranuclear gaze palsy |
Slow saccadic eye movements |
Supranuclear ophthalmoplegia |
Diplopia |
Blurred vision |
Color vision defect |
Photophobia |
Visual impairment |
| Disease(s) Associated with MAPT | ||||||||||
| late onset Parkinson's disease | ||||||||||
| Parkinson's disease | ||||||||||
| progressive supranuclear palsy |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
persistence of hyaloid vascular system |
decreased total retina thickness |
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| Availability | Mouse Genotype | ||||
| Mapttm1b(EUCOMM)Hmgu/Mapttm1b(EUCOMM)Hmgu | |||||
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 04/09/2024 MGI 6.23 |
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