Symbol Name ID |
Braf
Braf transforming gene MGI:88190 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the eye |
Optic atrophy |
Optic nerve dysplasia |
Hypertelorism |
Proptosis |
Strabismus |
Nystagmus |
Oculomotor apraxia |
Myopia |
Abnormality of vision |
Cerebral visual impairment |
Progressive visual loss |
Ptosis |
Disease(s) Associated with BRAF | |||||||||||||
cardiofaciocutaneous syndrome | |||||||||||||
cardiofaciocutaneous syndrome 1 | |||||||||||||
Noonan syndrome 7 | |||||||||||||
Noonan syndrome with multiple lentigines 3 |
Mouse Phenotypes | abnormal eye morphology |
cataract |
|
Availability | Mouse Genotype | ||
Braftm1Bbd/Braf+ | |||
Braftm2Cpri/Braf+ Tg(CMV-cre)1Cgn/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 09/03/2024 MGI 6.24 |
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