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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxg1
forkhead box G1
MGI:1347464
37 phenotypes from 3 alleles in 7 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Foxg1tm1(cre)Skm/Foxg1+
129(Cg)-Foxg1tm1(cre)Skm/J
no abnormal phenotype detected J:62916
Foxg1tm1(cre)Skm/Foxg1+
B6.129P2-Foxg1tm1(cre)Skm
abnormal cerebral cortex morphology J:128207
abnormal cerebral hemisphere morphology J:128207
abnormal telencephalon morphology J:128207
decreased cerebral cortex pyramidal cell number J:128207
decreased forebrain volume J:128207
decreased hippocampus volume J:128207
decreased striatum size J:128207
small thalamus J:128207
thin cerebral cortex J:128207
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * C57BL/6J
abnormal cerebral cortex pyramidal cell morphology J:235875
abnormal visual cortex morphology J:235875
abnormal visual evoked potential J:235875
decreased visual acuity J:235875
Foxg1tm1(cre)Skm/Foxg1+
involves: C57BL/6 * CBA
abnormal brain morphology J:128207
Foxg1tm1(cre)Skm/Foxg1tm1(cre)Skm
129(Cg)-Foxg1tm1(cre)Skm/J
perinatal lethality, complete penetrance J:62916
Foxg1tm1Chzh/Foxg1tm1Chzh
Tg(Fzd9-cre/ERT)1Chzh/0
involves: C57BL/6 * FVB
abnormal dentate gyrus morphology J:182692
abnormal neuronal precursor proliferation J:182692
abnormal radial glial cell morphology J:182692
Foxg1tm1M/Foxg1+
involves: C57BL/6 * CBA
abnormal brain morphology J:128207
Foxg1tm1M/Foxg1tm1M
involves: 129S1/Sv
abnormal neocortex morphology J:78115
abnormal neural tube mantle layer morphology J:78115
abnormal neuron differentiation J:78115
abnormal neuronal precursor proliferation J:78115
abnormal telencephalon morphology J:78115
Foxg1tm1M/Foxg1tm1M
involves: 129S1/Sv * C57BL/6J
abnormal cerebral cortex morphology J:26720
abnormal cerebral hemisphere morphology J:26720
abnormal cranium morphology J:26720
abnormal embryonic/fetal subventricular zone morphology J:26720
abnormal eye morphology J:26720
abnormal nasal placode morphology J:26720
abnormal olfactory epithelium morphology J:26720
abnormal retina morphology J:26720
abnormal retina neuronal layer morphology J:26720
abnormal telencephalon development J:26720
abnormal telencephalon morphology J:26720
cyanosis J:26720
neonatal lethality, complete penetrance J:26720
no spontaneous movement J:26720
respiratory distress J:26720
respiratory failure J:26720
small embryonic telencephalon J:26720
small olfactory bulb J:26720

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
04/30/2024
MGI 6.23
The Jackson Laboratory