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Symbol
Name
ID
Braf
Braf transforming gene
MGI:88190
Phenotype annotations related to vision/eye
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)

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
03/12/2024
MGI 6.23
The Jackson Laboratory