Symbol Name ID |
Nf2
neurofibromin 2 MGI:97307 |
Darker colors indicate more annotations |
Human Phenotypes | Facial palsy |
Lisch nodules |
Retinal hamartoma |
Disease(s) Associated with NF2 | |||
vestibular schwannomatosis |
Mouse Phenotypes | abnormal tooth development |
delayed tooth eruption |
failure of tooth eruption |
cleft upper lip |
cleft palate |
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Availability | Mouse Genotype | |||||
Nf2tm1Gth/Nf2+ | ||||||
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(Mpz-cre)3Brn/0 (conditional) |
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Nf2tm2Gth/Nf2tm2Gth Tg(Mpz-cre)#Brn/0 (conditional) |
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Nf2tm2Gth/Nf2tm2Gth Tg(rx3-icre)1Mjam/0 (conditional) |
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Nf2tm1Gth/Nf2tm2Gth Tg(Mpz-cre)2Brn/0 (conditional) |
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Nf2tm1Gth/Nf2tm2Gth Tg(Mpz-cre)#Brn/0 (conditional) |
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Nf2tm2Gth/Nf2+ Tg(Mpz-cre)#Brn/0 (conditional) |
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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