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Symbol Name ID |
Osbpl2
oxysterol binding protein-like 2 MGI:2442832 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sensorineural hearing impairment |
Tinnitus |
| Disease(s) Associated with OSBPL2 | ||
| autosomal dominant nonsyndromic deafness 67 |
| Mouse Phenotypes | abnormal inner hair cell kinocilium morphology |
abnormal outer hair cell kinocilium morphology |
abnormal cochlea morphology |
abnormal cochlear sensory epithelium morphology |
abnormal cochlear hair cell morphology |
abnormal orientation of cochlear hair cell stereociliary bundles |
abnormal organ of Corti supporting cell morphology |
small otic capsule |
abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
increased or absent distortion product otoacoustic emission threshold |
impaired hearing |
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| Availability | Mouse Genotype | ||||||||||||
| Osbpl2em1Cya/Osbpl2em1Cya | |||||||||||||
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 05/14/2024 MGI 6.23 |
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