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Symbol
Name
ID
Mapt
microtubule-associated protein tau
MGI:97180
Phenotype annotations related to vision/eye
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
Photophobia
Disease(s) Associated with MAPT
late onset Parkinson's disease
progressive supranuclear palsy

Mouse Phenotypes
abnormal retinal vasculature morphology
abnormal retinal blood vessel morphology
persistence of hyaloid vascular system
decreased total retina thickness
Availability Mouse Genotype
Mapttm1b(EUCOMM)Hmgu/Mapttm1b(EUCOMM)Hmgu

Contributing Projects:
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
10/15/2019
MGI 6.14
The Jackson Laboratory