|
Symbol Name ID |
Syne1
spectrin repeat containing, nuclear envelope 1 MGI:1927152 |
| Darker colors indicate more annotations |
| Human Phenotypes | Ankle clonus |
Spasticity |
Lower limb spasticity |
Peripheral axonal neuropathy |
Chronic axonal neuropathy |
Sensory axonal neuropathy |
Atrophy/Degeneration affecting the brainstem |
Abnormal cerebral white matter morphology |
Cerebellar atrophy |
Ataxia |
Dysmetria |
Gait ataxia |
Limb ataxia |
Clumsiness |
Abnormality of extrapyramidal motor function |
Fasciculations |
Upper motor neuron dysfunction |
Babinski sign |
Dysarthria |
Short attention span |
Intellectual disability |
Hyperreflexia |
Lower limb hyperreflexia |
Reduced tendon reflexes |
Areflexia |
Hyporeflexia |
Arm dystonia |
Gait disturbance |
Motor delay |
Delayed gross motor development |
Delayed ability to walk |
Motor polyneuropathy |
Polyneuropathy |
Impaired vibratory sensation |
Abnormal autonomic nervous system physiology |
| Disease(s) Associated with SYNE1 | |||||||||||||||||||||||||||||||||||
| arthrogryposis multiplex congenita-3 | |||||||||||||||||||||||||||||||||||
| autosomal recessive spinocerebellar ataxia 8 |
| Mouse Phenotypes | abnormal neuromuscular synapse morphology |
|
| Availability | Mouse Genotype | |
| Syne1tm1Rexu/Syne1tm1Rexu | ||
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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