Symbol Name ID |
Mios
meiosis regulator for oocyte development MGI:2182066 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | nervous system phenotype |
decreased brain size |
abnormal forebrain morphology |
decreased oligodendrocyte number |
abnormal oligodendrocyte physiology |
dysmyelination |
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Availability | Mouse Genotype | ||||||
Miostm1Pfw/Miostm1Pfw Tg(Nes-cre)1Kln/0 (conditional) |
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Miostm1Pfw/Miostm1Pfw Olig2tm2(TVA,cre)Rth/Olig2+ (conditional) |
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Miostm1Pfw/Miostm1Pfw Tg(Camk2a-cre)2Gsc/0 (conditional) |
* |
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 03/25/2025 MGI 6.24 |
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