Symbol Name ID |
Prnp
prion protein MGI:97769 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of eye movement |
Supranuclear gaze palsy |
Nystagmus |
Abnormal saccadic eye movements |
Slow saccadic eye movements |
Abnormality of ocular smooth pursuit |
Impaired smooth pursuit |
Jerky ocular pursuit movements |
Diplopia |
Visual impairment |
Disease(s) Associated with PRNP | ||||||||||
Creutzfeldt-Jakob disease | ||||||||||
fatal familial insomnia | ||||||||||
Gerstmann-Straussler-Scheinker syndrome | ||||||||||
Huntington's disease-like 1 |
Mouse Phenotypes | abnormal retina morphology |
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Availability | Mouse Genotype | |
Prnptm3Lnq/Prnptm3Lnq |
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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