|
Symbol Name ID |
Spg21
SPG21, maspardin MGI:106403 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dysphagia |
Spasticity |
Spastic paraparesis |
Spastic paraplegia |
Difficulty walking |
Thin corpus callosum |
Hypoplasia of the corpus callosum |
Periventricular white matter hyperintensities |
Cerebral atrophy |
Frontotemporal cerebral atrophy |
Abnormal cerebellum morphology |
Cerebellar atrophy |
Dysdiadochokinesis |
Incoordination |
Abnormality of extrapyramidal motor function |
Apraxia |
Athetosis |
Abnormal pyramidal sign |
Babinski sign |
Abnormality of peripheral nerve conduction |
Dysarthria |
Dysgraphia |
Akinetic mutism |
Personality disorder |
Mental deterioration |
Dementia |
Hyperreflexia |
Jaw hyperreflexia |
Primitive reflex |
Gait disturbance |
Global developmental delay |
Motor delay |
Peripheral neuropathy |
| Disease(s) Associated with SPG21 | |||||||||||||||||||||||||||||||||
| Mast syndrome |
| Mouse Phenotypes | abnormal neuron differentiation |
abnormal neuron morphology |
abnormal axon morphology |
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| Availability | Mouse Genotype | |||
| Spg21tm1Mchan/Spg21tm1Mchan | ||||
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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