About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:6163707
Allelic
Composition		 Foxg1tm1(cre)Skm/?
Gt(ROSA)26Sorem1(ptxA)Btar/?
Genetic
Background		 involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxg1tm1(cre)Skm mutation (2 available); any Foxg1 mutation (31 available)
Gt(ROSA)26Sorem1(ptxA)Btar mutation (0 available); any Gt(ROSA)26Sor mutation (1088 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
abnormal cochlear hair cell stereociliary bundle morphology ( J:236519 )
• at birth the apical hair cells show severe bundle misorientation

mortality/aging

nervous system
abnormal cochlear hair cell stereociliary bundle morphology ( J:236519 )
• at birth the apical hair cells show severe bundle misorientation

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
01/20/2026
MGI 6.24 		The Jackson Laboratory