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Symbol Name ID |
Nf2
neurofibromin 2 MGI:97307 |
| Darker colors indicate more annotations |
| Human Phenotypes | Lisch nodules |
Retinal hamartoma |
Abnormality of the eye |
Cataract |
Posterior subcapsular cataract |
Juvenile posterior subcapsular lenticular opacities |
Cortical cataract |
Abnormal optic nerve morphology |
Epiretinal membrane |
Remnants of the hyaloid vascular system |
Diplopia |
Reduced visual acuity |
Amblyopia |
Blindness |
Visual loss |
| Disease(s) Associated with NF2 | |||||||||||||||
| vestibular schwannomatosis |
| Mouse Phenotypes | retina pigment epithelium hyperplasia |
abnormal lens morphology |
abnormal lens epithelium morphology |
cataract |
failure of eyelid fusion |
abnormal optic cup morphology |
abnormal optic fissure morphology |
coloboma |
abnormal eye physiology |
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| Availability | Mouse Genotype | |||||||||
| Nf2tm2Gth/Nf2tm2Gth Tg(Mpz-cre)2Brn/0 (conditional) |
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| Nf2tm2Gth/Nf2tm2Gth Tg(Mpz-cre)3Brn/0 (conditional) |
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| Nf2tm2Gth/Nf2tm2Gth Tg(Nes-cre)1Kln/0 (conditional) |
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| Nf2tm2Gth/Nf2tm2Gth Tg(rx3-icre)1Mjam/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 04/30/2024 MGI 6.23 |
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