Symbol Name ID |
Fscn2
fascin actin-bundling protein 2 MGI:2443337 |
Darker colors indicate more annotations |
Human Phenotypes | Conductive hearing impairment |
Sensorineural hearing impairment |
Disease(s) Associated with FSCN2 | ||
retinitis pigmentosa |
Mouse Phenotypes | abnormal cochlear hair cell stereociliary bundle morphology |
decreased inner hair cell stereocilia number |
decreased outer hair cell stereocilia number |
short cochlear hair cell stereocilia |
cochlear outer hair cell degeneration |
abnormal cochlear outer hair cell physiology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
decreased distortion product otoacoustic emission amplitude |
increased susceptibility to age-related hearing loss |
impaired hearing |
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Availability | Mouse Genotype | |||||||||||
Fscn2ahl8/Fscn2ahl8 | ||||||||||||
Fscn2em1Fhan/Fscn2em1Fhan | ||||||||||||
Tg(RP24-180N9)2Kjn/0 |
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 05/28/2024 MGI 6.13 |
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