|
Symbol Name ID |
Nog
noggin MGI:104327 |
| * | Aspects of the system are reported to show a normal phenotype. |
| ! | Indicates phenotype varies with strain background. |
| Darker colors indicate more annotations |
| Human Phenotypes | Stapes ankylosis |
Conductive hearing impairment |
Bilateral conductive hearing impairment |
Progressive conductive hearing impairment |
Abnormal pinna morphology |
Low-set ears |
Posteriorly rotated ears |
Sensorineural hearing impairment |
Hearing abnormality |
| Disease(s) Associated with NOG | |||||||||
| brachydactyly type B2 | |||||||||
| craniosynostosis | |||||||||
| multiple synostoses syndrome 1 | |||||||||
| proximal symphalangism | |||||||||
| proximal symphalangism 1 | |||||||||
| tarsal-carpal coalition syndrome |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal middle ear ossicle morphology |
abnormal incus morphology |
abnormal malleus morphology |
abnormal stapes morphology |
fusion of middle ear ossicles |
abnormal ear development |
abnormal cochlea morphology |
increased cochlear inner hair cell number |
increased cochlear outer hair cell number |
decreased cochlea coiling |
abnormal middle ear morphology |
increased or absent threshold for auditory brainstem response |
impaired hearing |
conductive hearing loss |
|
| Availability | Mouse Genotype | |||||||||||||||
| Nogtm1Amc/Nogtm1Amc | ||||||||||||||||
| Nogtm1Amc/Nog+ | *! | ! | ||||||||||||||
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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