|
Symbol Name ID |
Zfyve26
zinc finger, FYVE domain containing 26 MGI:1924767 |
| Darker colors indicate more annotations |
| Human Phenotypes | Pseudobulbar paralysis |
Spasticity |
Lower limb spasticity |
Spastic paraplegia |
Upper limb spasticity |
Spastic gait |
Demyelinating peripheral neuropathy |
Peripheral axonal neuropathy |
Abnormal cerebral white matter morphology |
Hypoplasia of the corpus callosum |
Deep cerebral white matter hyperintensities |
Abnormal cerebellum morphology |
Ataxia |
Abnormality of extrapyramidal motor function |
Clonus |
Hand tremor |
Babinski sign |
Paraplegia |
Dysarthria |
Emotional lability |
Psychosis |
Atypical behavior |
Cognitive impairment |
Dementia |
Frontotemporal dementia |
Intellectual disability |
Hyperreflexia |
Lower limb hyperreflexia |
Gait disturbance |
Specific learning disability |
Seizure |
Impaired vibratory sensation |
| Disease(s) Associated with ZFYVE26 | ||||||||||||||||||||||||||||||||
| hereditary spastic paraplegia 15 |
| Mouse Phenotypes | delayed axon extension |
decreased brain weight |
Purkinje cell degeneration |
brain atrophy |
astrocytosis |
motor neuron degeneration |
axon degeneration |
|
| Availability | Mouse Genotype | |||||||
| Zfyve26tm1.1Cahb/Zfyve26tm1.1Cahb | ||||||||
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 04/23/2024 MGI 6.23 |
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