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Symbol Name ID |
Cln5
ceroid-lipofuscinosis, neuronal 5 MGI:2442253 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebral cortical atrophy |
Cerebellar atrophy |
Increased neuronal autofluorescent lipopigment |
Ataxia |
Dysdiadochokinesis |
Dysmetria |
Clumsiness |
Myoclonus |
Limb tremor |
Abnormal nervous system electrophysiology |
Dysarthria |
Motor deterioration |
Intellectual disability |
Loss of ambulation |
Developmental regression |
Seizure |
| Disease(s) Associated with CLN5 | ||||||||||||||||
| neuronal ceroid lipofuscinosis 5 |
| Mouse Phenotypes | abnormal brain morphology |
loss of GABAergic neurons |
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| Availability | Mouse Genotype | ||
| Cln5tm1Pltn/Cln5tm1Pltn | |||
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 04/30/2024 MGI 6.23 |
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