About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxj1
forkhead box J1
MGI:1347474
52 phenotypes from 7 alleles in 10 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Foxj1b2b774Clo/Foxj1b2b774Clo
C57BL/6J-Foxj1b2b774Clo
heart left ventricle hypertrophy J:175213
heart right ventricle hypertrophy J:175213
heterotaxia J:175213
situs inversus totalis J:175213
Foxj1tm1.1(cre/ERT2/GFP)Htg/Foxj1tm1.1(cre/ERT2/GFP)Htg
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * C57BL/6NCr
hydrocephaly J:213359
situs inversus J:213359
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk
Tg(FOXJ1-cre/ERT2)1Blh/0
involves: C57BL/6 * DBA
abnormal neuron differentiation J:174694
abnormal rostral migratory stream morphology J:174694
hydrocephaly J:174694
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk
Tg(FOXJ1-EGFP)85Leo/0
Tg(Nes-cre)1Kln/0
involves: C3H * C57BL/6 * C57BL/6J * SJL
abnormal neuron differentiation J:174694
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * SJL
abnormal brain morphology J:174694
hydrocephaly J:174694
Foxj1tm1Bph/Foxj1tm1Bph
involves: 129S1/Sv * 129X1/SvJ * Black Swiss
abnormal choroid plexus morphology J:50025
abnormal left-right axis patterning J:50025
absent brain ependyma motile cilia J:50025
absent oviduct epithelium motile cilium J:50025
absent respiratory motile cilia J:50025
absent sperm flagellum J:50025
cachexia J:50025
decreased birth body size J:50025
decreased fetal weight J:50025
dextrocardia J:50025
fetal growth retardation J:50025
heterotaxia J:50025
hydrocephaly J:50025
hypoactivity J:50025
infertility J:50025
lethality throughout fetal growth and development, incomplete penetrance J:50025
postnatal growth retardation J:50025
postnatal lethality, incomplete penetrance J:50025
situs inversus totalis J:50025
slow postnatal weight gain J:50025
Foxj1tm1Bph/Foxj1tm1Bph
involves: C57BL/6 * FVB/N
abnormal stomach position or orientation J:104135
aorta hypoplasia J:104135
normal cardiovascular system phenotype J:104135
lethality throughout fetal growth and development, incomplete penetrance J:104135
lung situs inversus J:104135
right pulmonary isomerism J:104135
right-sided stomach J:104135
Foxj1tm1Slb/Foxj1tm1Slb
involves: 129X1/SvJ
abnormal brain development J:154976
abnormal brain ependyma morphology J:154976
abnormal brain ventricle morphology J:154976
abnormal embryonic cilium location or orientation J:182741
abnormal olfactory bulb development J:154976
abnormal postnatal subventricular zone morphology J:154976
abnormal primitive node morphology J:182741
absent brain ependyma motile cilia J:73616
absent nodal flow J:182741
absent oviduct epithelium motile cilium J:73616
absent respiratory motile cilia J:73616
astrocytosis J:154976
decreased embryonic cilium length J:182741
dextrocardia J:73616
dilated lateral ventricles J:73616
hydrocephaly J:73616, J:154976
postnatal growth retardation J:73616
postnatal lethality, complete penetrance J:73616, J:174694
situs inversus J:73616
small olfactory bulb J:154976
transposition of great arteries J:73616
Foxj1tm1Slb/Foxj1tm1Slb
Tg(FOXJ1-EGFP)85Leo/0
involves: 129X1/SvJ * C3H * C57BL/6J
abnormal brain development J:154976
astrocytosis J:154976
Tg(CD2-Foxj1)#Stlp/0
C57BL/6-Tg(CD2-Foxj1)#Stlp
abnormal T cell physiology J:122222
decreased CD4-positive, alpha beta T cell number J:122222
decreased CD8-positive, alpha-beta T cell number J:122222
normal immune system phenotype J:122222
increased single-positive T cell number J:122222
lymphoid hypoplasia J:122222

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/23/2021
MGI 6.16
The Jackson Laboratory