|
Symbol Name ID |
Mag
myelin-associated glycoprotein MGI:96912 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Areflexia of lower limbs |
Hyporeflexia of lower limbs |
Spasticity |
Spastic paraparesis |
Spastic paraplegia |
Spastic dysarthria |
Spastic gait |
Ventriculomegaly |
Corpus callosum atrophy |
Cerebellar atrophy |
Dysmetria |
Titubation |
Abnormal pyramidal sign |
Babinski sign |
Dysarthria |
Cognitive impairment |
Intellectual disability |
Hyperreflexia |
Hyporeflexia |
Loss of ambulation |
Global developmental delay |
Peripheral neuropathy |
Impaired vibratory sensation |
Impaired distal vibration sensation |
| Disease(s) Associated with MAG | ||||||||||||||||||||||||
| hereditary spastic paraplegia 75 |
| Mouse Phenotypes | nervous system phenotype |
convulsive seizures |
abnormal oligodendrocyte morphology |
abnormal Schwann cell morphology |
abnormal axon morphology |
abnormal myelin sheath morphology |
tomacula |
axon degeneration |
abnormal myelination |
demyelination |
dysmyelination |
decreased prepulse inhibition |
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| Availability | Mouse Genotype | ||||||||||||
| Magtm1.1(KOMP)Vlcg/Magtm1.1(KOMP)Vlcg | |||||||||||||
| Magtm1Mtg/Magtm1Mtg | * | ||||||||||||
| Magtm1Pop/Magtm1Pop | |||||||||||||
| Magtm1Rod/Magtm1Rod | |||||||||||||
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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