Symbol Name ID |
Lyst
lysosomal trafficking regulator MGI:107448 |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Spastic paraplegia |
Abnormality of the nervous system |
Cerebellar atrophy |
Brain atrophy |
Atrophy of the spinal cord |
Neurodegeneration |
Ataxia |
Parkinsonism |
Tremor |
Cranial nerve paralysis |
Decreased nerve conduction velocity |
Cognitive impairment |
Dementia |
Intellectual disability |
Hyporeflexia |
Gait disturbance |
Inability to walk |
Specific learning disability |
Peripheral neuropathy |
Motor polyneuropathy |
Progressive peripheral neuropathy |
Sensory neuropathy |
Seizure |
Somatic sensory dysfunction |
Disease(s) Associated with LYST | |||||||||||||||||||||||||
Chediak-Higashi syndrome |
Mouse Phenotypes | abnormal hippocampal mossy fiber morphology |
abnormal hippocampus pyramidal cell layer |
ectopic hippocampus pyramidal cells |
ectopic Bergmann glia cells |
decreased Purkinje cell number |
ectopic Purkinje cell |
ectopic cerebellar granule cells |
decreased prepulse inhibition |
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Availability | Mouse Genotype | ||||||||
Lystbg-2J/Lystbg-2J | |||||||||
Lystbg-J/Lystbg-J | |||||||||
Lystbg/Lystbg | |||||||||
Lysttm1b(EUCOMM)Wtsi/Lysttm1b(EUCOMM)Wtsi |
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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