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Symbol
Name
ID
Foxj1
forkhead box J1
MGI:1347474
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Noncommunicating hydrocephalus
Disease(s) Associated with FOXJ1
primary ciliary dyskinesia 43

Mouse Phenotypes
absent brain ependyma motile cilia
abnormal neuron differentiation
abnormal brain morphology
abnormal brain development
abnormal olfactory bulb development
abnormal rostral migratory stream morphology
hydrocephaly
abnormal brain ventricle morphology
abnormal brain ependyma morphology
dilated lateral ventricles
abnormal choroid plexus morphology
small olfactory bulb
abnormal postnatal subventricular zone morphology
astrocytosis
Availability Mouse Genotype
Foxj1tm1.1(cre/ERT2/GFP)Htg/Foxj1tm1.1(cre/ERT2/GFP)Htg
Foxj1tm1Bph/Foxj1tm1Bph
Foxj1tm1Slb/Foxj1tm1Slb
Foxj1tm1Slb/Foxj1tm1Slb
Tg(FOXJ1-EGFP)85Leo/0
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk
Tg(FOXJ1-cre/ERT2)1Blh/0  (conditional)
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk
Tg(Nes-cre)1Kln/0  (conditional)
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk
Tg(FOXJ1-EGFP)85Leo/0
Tg(Nes-cre)1Kln/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
02/23/2021
MGI 6.16
The Jackson Laboratory