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Symbol Name ID |
Nf2
neurofibromin 2 MGI:97307 |
| Darker colors indicate more annotations |
| Human Phenotypes | Vestibular schwannoma |
Bilateral vestibular schwannoma |
Unilateral vestibular schwannoma |
Vertigo |
Sensorineural hearing impairment |
Hearing impairment |
Tinnitus |
| Disease(s) Associated with NF2 | |||||||
| vestibular schwannomatosis |
| Mouse Phenotypes | abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
sensorineural hearing loss |
increased susceptibility to otitis media |
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| Availability | Mouse Genotype | ||||
| Nf2tm2Gth/Nf2tm2Gth Tg(Mpz-cre)1Brn/0 (conditional) |
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| Nf2tm2Gth/Nf2tm2Gth Tg(Mpz-cre)2Brn/0 (conditional) |
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| Nf2tm2Gth/Nf2tm2Gth Tg(Postn-cre)1Sjc/0 (conditional) |
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| Nf2tm1Gth/Nf2tm2Gth Tg(Mpz-cre)2Brn/0 (conditional) |
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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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