|
Symbol Name ID |
Ttpa
tocopherol (alpha) transfer protein MGI:1354168 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of visual evoked potentials |
Cerebellar atrophy |
Ataxia |
Dysdiadochokinesis |
Dysmetria |
Progressive cerebellar ataxia |
Clumsiness |
Tremor |
Abnormal pyramidal sign |
Hemiplegia/hemiparesis |
Delayed somatosensory central conduction time |
Abnormality of speech or vocalization |
Dysarthria |
Perseverative thought |
Short term memory impairment |
Mental deterioration |
Areflexia |
Dystonia |
Gait disturbance |
Developmental regression |
Peripheral neuropathy |
Sensory neuropathy |
Impaired proprioception |
Positive Romberg sign |
| Disease(s) Associated with TTPA | ||||||||||||||||||||||||
| familial isolated deficiency of vitamin E |
| Mouse Phenotypes | abnormal spinal cord ventral horn morphology |
neurodegeneration |
abnormal somatosensory cortex physiology |
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| Availability | Mouse Genotype | |||
| Ttpatm1Hsz/Ttpatm1Hsz | ||||
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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