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Symbol Name ID |
Nf2
neurofibromin 2 MGI:97307 |
| Darker colors indicate more annotations |
| Human Phenotypes | Urticaria |
Axillary freckling |
Inguinal freckling |
Hyperpigmentation of the skin |
Cafe-au-lait spot |
Neoplasm of the skin |
Neurofibroma |
Peripheral schwannoma |
| Disease(s) Associated with NF2 | ||||||||
| gastrointestinal stromal tumor | ||||||||
| vestibular schwannomatosis |
| Mouse Phenotypes | increased fibroadenoma incidence |
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| Availability | Mouse Genotype | |
| Nf2tm1Gth/Nf2+ | ||
| Nf2tm2Gth/Nf2tm2Gth Tg(Mpz-cre)3Brn/0 (conditional) |
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| Nf2tm2Gth/Nf2+ Tg(Mpz-cre)#Brn/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 04/09/2024 MGI 6.23 |
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