Foxg1 Phenotype Annotations

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

Allelic Composition Genetic Background	Annotated Term	Reference
Foxg1^tm1(cre)Skm/Foxg1⁺ 129(Cg)-Foxg1^tm1(cre)Skm/J	no abnormal phenotype detected	J:62916
Foxg1^tm1(cre)Skm/Foxg1⁺ B6.129P2-Foxg1^tm1(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
Foxg1^tm1(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
Foxg1^tm1(cre)Skm/Foxg1⁺ involves: C57BL/6 * CBA	abnormal brain morphology	J:128207
Foxg1^tm1(cre)Skm/Foxg1^tm1(cre)Skm 129(Cg)-Foxg1^tm1(cre)Skm/J	perinatal lethality, complete penetrance	J:62916
Foxg1^tm1Chzh/Foxg1^tm1Chzh 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
Foxg1^tm1M/Foxg1⁺ involves: C57BL/6 * CBA	abnormal brain morphology	J:128207
Foxg1^tm1M/Foxg1^tm1M 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
Foxg1^tm1M/Foxg1^tm1M 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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