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Symbol
Name
ID
Fbxw7
F-box and WD-40 domain protein 7
MGI:1354695
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Astigmatism
Strabismus
Cerebral visual impairment
Disease(s) Associated with FBXW7
developmental delay, hypotonia, and impaired language

Mouse Phenotypes
eyelids open at birth
Availability Mouse Genotype
Fbxw7tm1.1Iken/Fbxw7+
Fbxw7tm1Itom/Fbxw7+
Tg(Pgk1-cre)1Lni/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
08/02/2024
MGI 6.24
The Jackson Laboratory