|
Symbol Name ID |
Opa3
optic atrophy 3 MGI:2686271 |
| Darker colors indicate more annotations |
| Human Phenotypes | Areflexia of lower limbs |
Absent Achilles reflex |
Extrapyramidal muscular rigidity |
Spasticity |
Spastic paraparesis |
Cerebellar atrophy |
Ataxia |
Abnormality of extrapyramidal motor function |
Choreoathetosis |
Chorea |
Tremor |
Postural tremor |
Resting tremor |
Babinski sign |
Dysarthria |
Cognitive impairment |
Intellectual disability |
Hyperreflexia |
Reduced tendon reflexes |
Areflexia |
Gait disturbance |
Unsteady gait |
Dyslexia |
Somatic sensory dysfunction |
Paresthesia |
Positive Romberg sign |
| Disease(s) Associated with OPA3 | ||||||||||||||||||||||||||
| 3-methylglutaconic aciduria type 3 | ||||||||||||||||||||||||||
| optic atrophy 3 |
| Mouse Phenotypes | decreased retina ganglion cell number |
abnormal optic nerve morphology |
axon degeneration |
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| Availability | Mouse Genotype | |||
| Opa3m1Votr/Opa3m1Votr | ||||
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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