|
Symbol Name ID |
Ctsf
cathepsin F MGI:1861434 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ventriculomegaly |
Cerebral cortical atrophy |
Diffuse cerebral atrophy |
Cerebellar atrophy |
Neuronal loss in central nervous system |
Ataxia |
Gait ataxia |
Abnormality of extrapyramidal motor function |
Myoclonus |
Tremor |
Babinski sign |
Dysarthria |
Depression |
Emotional lability |
Confusion |
Mental deterioration |
Dementia |
Hyperreflexia |
Primitive reflex |
Seizure |
Bilateral tonic-clonic seizure |
Focal-onset seizure |
| Disease(s) Associated with CTSF | ||||||||||||||||||||||
| neuronal ceroid lipofuscinosis 13 |
| Mouse Phenotypes | decreased brain weight |
gliosis |
abnormal motor neuron morphology |
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| Availability | Mouse Genotype | |||
| Ctsftm1Hap/Ctsftm1Hap | ||||
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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