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Symbol Name ID |
Mobp
myelin-associated oligodendrocytic basic protein MGI:108511 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Amyotrophic lateral sclerosis |
Neuronal loss in central nervous system |
Parkinsonism |
Language impairment |
Irritability |
Diminished motivation |
Apathy |
Abnormal sexual behavior |
Inappropriate laughter |
Personality changes |
Polyphagia |
Disinhibition |
Hyperorality |
Dementia |
Frontal lobe dementia |
Frontotemporal dementia |
Primitive reflex |
| Disease(s) Associated with MOBP | |||||||||||||||||
| frontotemporal dementia |
| Mouse Phenotypes | nervous system phenotype |
abnormal myelination |
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| Availability | Mouse Genotype | ||
| Mobptm1Irg/Mobptm1Irg | * | ||
| Mobptm1Sak/Mobptm1Sak | |||
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 08/02/2024 MGI 6.24 |
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