|
Symbol Name ID |
Spart
spartin MGI:2139806 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Drooling |
Ankle clonus |
Dysphagia |
Spasticity |
Lower limb spasticity |
Spastic paraparesis |
Spastic paraplegia |
Upper limb spasticity |
Spastic dysarthria |
Spastic gait |
Difficulty walking |
Abnormal brain morphology |
Abnormal cerebellum morphology |
Cerebellar atrophy |
Dysmetria |
Slurred speech |
Speech apraxia |
Knee clonus |
Babinski sign |
Delayed speech and language development |
Dysarthria |
Emotional lability |
Anxiety |
Panic attack |
Psychosis |
Hallucinations |
Cognitive impairment |
Intellectual disability, mild |
Sleep abnormality |
Hyperreflexia |
Global developmental delay |
Motor delay |
Specific learning disability |
Impaired vibratory sensation |
Impaired vibration sensation at ankles |
| Disease(s) Associated with SPART | ||||||||||||||||||||||||||||||||||||
| Troyer syndrome |
| Mouse Phenotypes | nervous system phenotype |
abnormal axon morphology |
abnormal dendrite morphology |
|
| Availability | Mouse Genotype | |||
| Sparttm1.1Xen/Sparttm1.1Xen | * | |||
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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