Symbol Name ID |
Snap25
synaptosomal-associated protein 25 MGI:98331 |
Darker colors indicate more annotations |
Human Phenotypes | Aganglionic megacolon |
Difficulty walking |
Fatigable weakness |
Alzheimer disease |
Ataxia |
Echolalia |
Dysarthria |
Poor speech |
Intellectual disability |
Areflexia |
Gait disturbance |
Developmental regression |
Global developmental delay |
Delayed ability to walk |
Specific learning disability |
Seizure |
Impaired pain sensation |
Disease(s) Associated with SNAP25 | |||||||||||||||||
congenital myasthenic syndrome 18 | |||||||||||||||||
Down syndrome |
Mouse Phenotypes | seizures |
convulsive seizures |
myoclonus |
abnormal brain morphology |
abnormal hippocampus CA3 region morphology |
abnormal cerebral cortex morphology |
abnormal CNS synaptic transmission |
abnormal miniature excitatory postsynaptic currents |
decreased prepulse inhibition |
abnormal PNS synaptic transmission |
abnormal endplate potential |
decreased synaptic glutamate release |
decreased paired-pulse facilitation |
enhanced paired-pulse facilitation |
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Availability | Mouse Genotype | ||||||||||||||
Snap25tm1.1Bark/Snap25tm1.1Bark | |||||||||||||||
Snap25tm1Bark/Snap25tm1Bark | |||||||||||||||
Snap25tm1Mcw/Snap25tm1Mcw | |||||||||||||||
Snap25tm1Mtaka/Snap25tm1Mtaka | |||||||||||||||
Snap25tm2Mcw/Snap25tm2Mcw | |||||||||||||||
Snap25Bdr/Snap25+ |
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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