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Symbol
Name
ID
Nf2
neurofibromin 2
MGI:97307
Phenotype annotations related to craniofacial
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
Availability Mouse Genotype
Nf2tm1Gth/Nf2+
Nf2tm2Gth/Nf2tm2Gth
Tg(Mpz-cre)1Brn/0  (conditional)
Nf2tm2Gth/Nf2tm2Gth
Tg(Mpz-cre)2Brn/0  (conditional)
Nf2tm2Gth/Nf2tm2Gth
Tg(Mpz-cre)3Brn/0  (conditional)
Nf2tm2Gth/Nf2tm2Gth
Tg(Mpz-cre)#Brn/0  (conditional)
Nf2tm2Gth/Nf2tm2Gth
Tg(rx3-icre)1Mjam/0  (conditional)
Nf2tm1Gth/Nf2tm2Gth
Tg(Mpz-cre)2Brn/0  (conditional)
Nf2tm1Gth/Nf2tm2Gth
Tg(Mpz-cre)#Brn/0  (conditional)
Nf2tm2Gth/Nf2+
Tg(Mpz-cre)#Brn/0  (conditional)

Contributing Projects:
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
The Jackson Laboratory