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Symbol Name ID |
Foxi1
forkhead box I1 MGI:1096329 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Incomplete partition of the cochlea type II |
Enlarged vestibular aqueduct |
Sensorineural hearing impairment |
| Disease(s) Associated with FOXI1 | |||
| autosomal recessive nonsyndromic deafness 4 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
inner ear cyst |
abnormal inner ear morphology |
abnormal cochlea morphology |
absent cochlear modiolus |
absent cochlea |
abnormal common crus morphology |
dilated lateral semicircular canal |
dilated posterior semicircular canal |
enlarged utricle |
enlarged vestibular saccule |
absent inner ear vestibule |
abnormal membranous labyrinth morphology |
dilated endolymphatic duct |
dilated endolymphatic sac |
absent otoliths |
absent endocochlear potential |
impaired hearing |
deafness |
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| Availability | Mouse Genotype | |||||||||||||||||||
| Foxi1tm1Sven/Foxi1tm1Sven | ||||||||||||||||||||
| Foxi1tm1Sven/Foxi1+ | * | |||||||||||||||||||
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 04/16/2024 MGI 6.23 |
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