Mios Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mios
meiosis regulator for oocyte development
MGI:2182066

7 phenotypes from 1 allele in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mios^tm1Pfw/Mios^tm1Pfw Olig2^{tm2(TVA,cre)Rth}/Olig2⁺ involves: 129 * C57BL/6	abnormal oligodendrocyte physiology	J:320720
	normal behavior/neurological phenotype	J:320720
	decreased oligodendrocyte number	J:320720
	dysmyelination	J:320720
Mios^tm1Pfw/Mios^tm1Pfw Tg(Camk2a-cre)2Gsc/0 involves: C57BL/6 * FVB/N	normal nervous system phenotype	J:320720
Mios^tm1Pfw/Mios^tm1Pfw Tg(Nes-cre)1Kln/0 involves: C57BL/6 * SJL	abnormal forebrain morphology	J:320720
	decreased brain size	J:320720
	decreased oligodendrocyte number	J:320720
	dysmyelination	J:320720

Contributing Projects: 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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