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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Foxg1
forkhead box G1
MGI:1347464
222 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Actbtm1.1Erv/Actbtm1.1Erv
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * FVB/N 		normal hearing/vestibular/ear phenotype J:167543
postnatal lethality, incomplete penetrance J:167543
Aifm1tm2Pngr/Y
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		abnormal enzyme/coenzyme level J:112874
abnormal mitochondrial morphology J:112874
abnormal mitochondrial physiology J:112874
decreased mitochondrial fission J:112874
decreased neuron apoptosis J:112874
increased neuron apoptosis J:112874
lethality throughout fetal growth and development, incomplete penetrance J:112874
thin cerebral cortex J:112874
Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr
Aifm1tm2Pngr/Y
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ 		abnormal mitochondrial physiology J:112874
decreased neuron apoptosis J:112874
increased neuron apoptosis J:112874
thickened cerebral cortex J:112874
Atrxtm1Rjg/Y
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * C57BL/6 * FVB/N 		abnormal suckling behavior J:95953
absent dentate gyrus J:95953
absent gastric milk in neonates J:95953
decreased birth body size J:95953
decreased hippocampus pyramidal cell number J:95953
loss of cortex neurons J:95953
loss of hippocampal neurons J:95953
postnatal lethality, complete penetrance J:95953
Bmp2tm1Brd/Bmp2tm1.1Mis
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J 		normal hearing/vestibular/ear phenotype J:156945
Bmp4tm1Blh/Bmp4tm4Blh
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * Black Swiss * C57BL/6 * SJL 		abnormal endolymphatic duct morphology J:136636
abnormal scala media morphology J:136636
abnormal semicircular canal ampulla morphology J:136636
abnormal semicircular canal morphology J:136636
abnormal utricle morphology J:136636
abnormal vestibular saccule morphology J:136636
absent semicircular canals J:136636
Bmp4tm3Blh/Bmp4+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac 		prenatal lethality, incomplete penetrance J:83123
Bmp4tm3Blh/Bmp4tm3Blh
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac 		abnormal eye development J:83123
abnormal face development J:83123
abnormal snout morphology J:83123
embryonic lethality during organogenesis, complete penetrance J:83123
normal nervous system phenotype J:83123
retrognathia J:83123
Bptftm1.1Cwu/Bptftm1.1Cwu
Foxg1tm1(cre)Skm/?
involves: 129P2/OlaHsd-Hprtb-m3 * 129S1/Sv-Oca2+ Tyr+ Kitl+ 		abnormal olfactory sensory neuron morphology J:217534
perinatal lethality, complete penetrance J:217534
Bsndtm1Tjj/Bsndtm1Tjj
Foxg1tm1(cre)Skm/Foxg1+
involves: 129/Sv * 129P2/OlaHsd * 129X1/SvJ * C57BL/6 		collapsed Reissner membrane J:143314
dehydration J:143314
postnatal lethality, complete penetrance J:143314
Cdc42tm1Yizh/Cdc42tm1Yizh
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		abnormal embryonic neuroepithelium morphology J:116100
abnormal eye development J:116100
abnormal folding of telencephalic vesicles J:116100
abnormal telencephalon development J:116100
holoprosencephaly J:116100
lethality throughout fetal growth and development, complete penetrance J:116100
small embryonic telencephalon J:116100
Celsr3tm1Agof/Celsr3tm2Agof
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		abnormal brain internal capsule morphology J:134879
abnormal corticospinal tract morphology J:134879
absent anterior commissure J:134879
Chd7Gt(S20-7E1)Sor/Chd7tm1.1Dmm
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * C57BL/6 * Swiss Webster 		abnormal cochlea morphology J:164582
abnormal cochlear sensory epithelium morphology J:310063
abnormal crista ampullaris morphology J:164582
abnormal ear development J:164582
abnormal inner ear vestibule morphology J:164582
abnormal neuronal precursor cell number J:164582
abnormal neuronal precursor proliferation J:164582
abnormal suckling behavior J:164582
abnormal vestibulocochlear ganglion morphology J:164582, J:310063
absent lateral semicircular canal J:164582
absent posterior semicircular canal J:164582
absent utricle J:164582
absent vestibular saccule J:164582
decreased cochlea coiling J:164582
decreased superior semicircular canal size J:164582
increased cochlear outer hair cell number J:310063
neonatal lethality, complete penetrance J:164582
ocular hypertelorism J:164582
short snout J:164582
small endolymphatic duct J:164582
Chd7tm1.1Dmm/Chd7+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * C57BL/6 * Swiss Webster 		abnormal ear development J:164582
abnormal vestibulocochlear ganglion morphology J:164582
decreased lateral semicircular canal size J:164582
Chd7tm1.1Dmm/Chd7tm1.1Dmm
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac 		abnormal lens development J:231044
absent optic cup J:231044
Dll1tm1Mjo/Dll1tm1Mjo
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * C57BL/6J 		abnormal cochlear hair cell morphology J:107414
abnormal utricular macula morphology J:107414
abnormal vestibular saccular macula morphology J:107414
decreased cochlea coiling J:107414
increased cochlear inner hair cell number J:107414
increased cochlear outer hair cell number J:107414
Fgf8tm1.1Mrt/Fgf8tm1.4Mrt
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		increased neuron apoptosis J:111586
Fgf8tm1.1Mrt/Fgf8tm1.4Mrt
Foxg1tm1M/Foxg1+
involves: 129P2/OlaHsd 		abnormal neuron apoptosis J:111586
Fgf8tm1.2Mrt/Fgf8tm1.3Mrt
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		abnormal cochlear sensory epithelium morphology J:122378
abnormal forebrain development J:122378
abnormal patterning of the organ of Corti J:122378
abnormal pillar cell differentiation J:122378
abnormal pillar cell morphology J:122378
absent pillar cells J:122378
perinatal lethality, complete penetrance J:122378
Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		increased neuron apoptosis J:111586
Fgfr1tm1Upir/Fgfr1tm1.1Upir
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * ICR 		abnormal cochlea morphology J:78879
abnormal cochlear hair cell development J:78879
abnormal cochlear sensory epithelium morphology J:78879
abnormal organ of Corti morphology J:78879
abnormal orientation of inner hair cell stereociliary bundles J:78879
absent cochlear outer hair cells J:78879
absent organ of Corti supporting cells J:78879
decreased cochlear hair cell number J:78879
increased cochlear inner hair cell number J:78879
neonatal lethality, complete penetrance J:78879
Fgfr1tm1Upir/Fgfr1tm1Upir
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * ICR 		abnormal cochlear sensory epithelium morphology J:78879
abnormal organ of Corti morphology J:78879
neonatal lethality, complete penetrance J:78879
Fgfr2tm1Dor/Fgfr2+
Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm1Jpa/Fgfr1tm1Jpa
Frs3tm1Jheb/Frs3tm1Jheb
involves: 129 		normal cellular phenotype J:242687
normal nervous system phenotype J:242687
Fgfr2tm1Dor/Fgfr2tm1Dor
Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm6.1Jrt/Fgfr1tm1Jpa
involves: 129 		normal nervous system phenotype J:242687
Fgfr2tm1Dor/Fgfr2tm1Dor
Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm1Jpa/Fgfr1tm1Jpa
Frs3tm1Jheb/Frs3tm1Jheb
involves: 129 		absent telencephalon J:242687
Fgfr2tm1Dor/Fgfr2tm1Dor
Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm3.1Sor/Fgfr1tm1Jpa
Frs3tm1Jheb/Frs3tm1Jheb
involves: 129 		absent telencephalon J:242687
normal cellular phenotype J:242687
increased cell death J:242687
Fgfr2tm1Dor/Fgfr2tm1Dor
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm1Jpa/Fgfr1tm1Jpa
involves: 129 		frontonasal prominence hypoplasia J:242687
microphthalmia J:242687
telencephalon hypoplasia J:242687
Fgfr2tm1Dor/Fgfr2tm1Dor
Foxg1tm1(cre)Skm/Foxg1+
Fgfr1tm3.1Sor/Fgfr1tm1Jpa
involves: 129 		abnormal lateral ganglionic eminence morphology J:242687
abnormal medial ganglionic eminence morphology J:242687
frontonasal prominence hypoplasia J:242687
microphthalmia J:242687
telencephalon hypoplasia J:242687
Foxg1tm1(cre)Skm/Foxg1+
Lrp2tm1Tew/Lrp2tm1Tew
involves: 129P2/OlaHsd 		abnormal dendrite morphology J:238249
abnormal eye morphology J:238249
abnormal intraocular pressure J:238249
abnormal lens morphology J:238249
abnormal optic nerve morphology J:238249
abnormal placement of pupils J:238249
abnormal posterior eye segment morphology J:238249
abnormal retina bipolar cell morphology J:238249
abnormal retina pigment epithelium morphology J:238249
abnormal retina pigmentation J:238249
abnormal sclera morphology J:238249
absent corpus callosum J:238249
decreased cell proliferation J:238249
decreased retina ganglion cell number J:238249
decreased total retina thickness J:238249
high myopia J:238249
increased retina apoptosis J:238249
macrophthalmia J:238249
ocular hypotelorism J:238249
sclera thinning J:238249
thin retina inner nuclear layer J:238249
thin retina inner plexiform layer J:238249
thin retina outer nuclear layer J:238249
Foxg1tm1(cre)Skm/Foxg1+
Frs2tm1Fwan/Frs2tm1Fwan
Frs3tm1Jheb/Frs3tm1Jheb
involves: 129 * Swiss Webster 		abnormal cortical ventricular zone morphology J:242687
abnormal embryonic/fetal subventricular zone morphology J:242687
abnormal lateral ganglionic eminence morphology J:242687
abnormal medial ganglionic eminence morphology J:242687
normal cellular phenotype J:242687
frontonasal prominence hypoplasia J:242687
microphthalmia J:242687
normal nervous system phenotype J:242687
telencephalon hypoplasia J:242687
Foxg1tm1(cre)Skm/?
Gt(ROSA)26Sorem1(ptxA)Btar/?
involves: 129P2/OlaHsd * C57BL/6J 		abnormal cochlear hair cell stereociliary bundle morphology J:236519
neonatal lethality, complete penetrance J:236519
Foxg1tm1(tTA)Lai/Foxg1+
Tg(tetO-Gsx2,-EGFP)1Kc/0
involves: 129S1/Sv 		abnormal brain morphology J:154936
abnormal lateral ganglionic eminence morphology J:154936
abnormal olfactory bulb morphology J:154936
abnormal telencephalon development J:154936
Foxg1tm1(tTA)Lai/Foxg1tm1M
Tg(tetO-Foxg1)1Lai/0
involves: 129S1/Sv * C57BL/6 		abnormal basal ganglion morphology J:78115
abnormal neural tube mantle layer morphology J:78115
abnormal neuron differentiation J:78115
abnormal telencephalon morphology J:78115
normal nervous system phenotype J:78115
Foxg1tm1.1(cre)Ddmo/Foxg1+
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1atm1a(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N 		telencephalon hypoplasia J:335489
Foxg1tm1.1(cre)Ddmo/Foxg1+
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1atm1c(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N 		telencephalon hypoplasia J:335489
Foxg1tm1.1(cre)Ddmo/Foxg1+
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1atm1d(EUCOMM)Hmgu/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N 		telencephalon hypoplasia J:335489
Foxg1tm1.1(cre)Ddmo/0
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
Polr1aem1Knwea/Polr1atm1c(EUCOMM)Hmgu
involves: 129S1/Sv * 129T/Sv * 129X1/SvJ * C57BL/6N 		telencephalon hypoplasia J:335489
Gt(ROSA)26Sortm1(Cacna1c*)Red/Gt(ROSA)26Sor+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ 		abnormal neuron morphology J:199433
Gt(ROSA)26Sortm1(RARA*)Soc/Gt(ROSA)26Sortm1(RARA*)Soc
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		abnormal medial ganglionic eminence morphology J:135403
telencephalon hypoplasia J:135403
Gt(ROSA)26Sortm1(Tbx1/GFP)Bem/Gt(ROSA)26Sor+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * C57BL/6 * SJL 		abnormal cochlea morphology J:204435
abnormal common crus morphology J:204435
abnormal endolymphatic duct morphology J:204435
abnormal forebrain morphology J:204435
abnormal frontonasal prominence morphology J:204435
abnormal geniculate ganglion morphology J:204435
abnormal glossopharyngeal ganglion morphology J:204435
abnormal nasal placode morphology J:204435
abnormal optic vesicle formation J:204435
abnormal trigeminal ganglion morphology J:204435
abnormal vagus ganglion morphology J:204435
absent lateral semicircular canal J:204435
absent utricle J:204435
absent vestibular saccule J:204435
athymia J:204435
cochlear ganglion degeneration J:204435
perinatal lethality, complete penetrance J:204435
vestibular ganglion degeneration J:204435
Igs1tm11(CAG-Bgeo,-Edn2)Nat/Igs1+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 		cleft palate J:201133
failure of eyelid fusion J:201133
postnatal lethality J:201133
Jag1tm1Grid/Jag1tm2Grid
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 		abnormal cochlea morphology J:115783
abnormal cochlear hair cell morphology J:115783
abnormal cochlear hair cell number J:115783
abnormal cochlear outer hair cell morphology J:115783
abnormal crista ampullaris morphology J:115783
abnormal lateral semicircular canal morphology J:115783
abnormal superior semicircular canal morphology J:115783
abnormal utricular macula morphology J:115783
abnormal vestibular saccule morphology J:115783
absent cochlear hair cells J:115783
absent semicircular canals J:115783
absent tunnel of Corti J:115783
decreased cochlea coiling J:115783
normal hearing/vestibular/ear phenotype J:115783
perinatal lethality, complete penetrance J:115783
small utricle J:115783
Lmo4tm1Gan/Lmo4tm2.1Gan
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J 		abnormal inner ear morphology J:156733
abnormal semicircular canal ampulla morphology J:156733
absent semicircular canals J:156733
Lmo4tm2.1Gan/Lmo4tm2.1Gan
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J 		abnormal inner ear morphology J:156733
abnormal semicircular canal ampulla morphology J:156733
absent semicircular canals J:156733
Mafbtm1.1Good/Mafbtm1Jeng
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL 		apnea J:207904
normal hearing/vestibular/ear phenotype J:207904
neonatal lethality, complete penetrance J:207904
normal nervous system phenotype J:207904
Notch1tm1Grid/Notch1tm2Rko
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * C57BL/6J * Swiss Webster 		decreased organ of Corti supporting cell number J:132241
increased cochlear inner hair cell number J:132241
Notch2tm3Grid/Notch2tm3Grid
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 		abnormal nervous system physiology J:130929
abnormal olfactory epithelium morphology J:130929
abnormal sensory neuron morphology J:130929
decreased body weight J:130929
increased apoptosis J:130929
increased neuron apoptosis J:130929
increased neuronal precursor cell number J:130929
neuron degeneration J:130929
premature death J:130929
small pituitary gland J:130929
Ntf3tm1Esm/Ntf3tm1Esm
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv 		abnormal nervous system tract morphology J:81563
abnormal vision J:81563
decreased CNS synapse formation J:81563
Olig2tm1Qrlu/Olig2tm1Qrlu
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 		abnormal myelination J:105071
Pbx1tm1Koss/Pbx1tm1Koss
Pbx2tm1Mlc/Pbx2+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S/Sv 		abnormal maxillary shelf morphology J:178316
abnormal nasal capsule morphology J:178316
absent premaxilla J:178316
bilateral cleft upper lip J:178316
cleft palate J:178316
neonatal lethality, complete penetrance J:178316
Pbx1tm1Koss/Pbx1tm1Koss
Pbx2tm1Mlc/Pbx2tm1Mlc
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S/Sv 		bilateral cleft upper lip J:178316
decreased apoptosis J:178316
Pbx1tm1Koss/Pbx1tm1Koss
Pbx3tm1Mlc/Pbx3+
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		cleft palate J:178316
cleft upper lip J:178316
Pbx1tm1Mlc/Pbx1+
Wnt9btm1Amc/Wnt9btm1Amc
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S6/SvEvTac * 129X1/SvJ 		bilateral cleft upper lip J:178316
cleft palate J:178316
Rhoatm1Yuyo/Rhoatm1Yuyo
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd 		abnormal brain development J:172044
exencephaly J:172044
increased neuronal precursor cell number J:172044
Six3tm3Gco/Six3tm3Gco
Foxg1tm1(cre)Skm/Foxg1+
involves: 129S1/Sv * C57BL/6 		holoprosencephaly J:140315
Slc12a2tm1.1Jheb/Slc12a2tm1.1Jheb
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal crista ampullaris morphology J:201156
abnormal inner ear morphology J:201156
circling J:201156
collapsed Reissner membrane J:201156
hyperactivity J:201156
utricular degeneration J:201156
vestibular saccular degeneration J:201156
Smarca1tm1.1Pick/Y
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S4/SvJae * CD-1 		normal nervous system phenotype J:183998
Sp8tm1Smb/Sp8tm2Smb
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ 		abnormal face development J:200761
abnormal telencephalon morphology J:200761
cleft palate J:200761
cleft upper lip J:200761
exencephaly J:200761
midline facial cleft J:200761
normal vision/eye phenotype J:200761
Sp8tm2.1Aman/Sp8tm2.1Aman
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * C57BL/6 		abnormal basal ganglion morphology J:160653
abnormal brain internal capsule morphology J:160653
abnormal cortical plate morphology J:160653
abnormal craniofacial morphology J:160653
abnormal forebrain development J:160653
abnormal lateral ventricle morphology J:160653
abnormal neuronal precursor proliferation J:160653
abnormal olfactory bulb development J:160653
abnormal telencephalon development J:160653
forebrain hypoplasia J:160653
holoprosencephaly J:160653
increased neuron apoptosis J:160653
neonatal lethality, complete penetrance J:160653
telencephalon hypoplasia J:160653
thin cortical plate J:160653
Tbx1tm2.1Bem/Tbx1tm2.2Bem
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * C57BL/6J * SJL * Swiss Webster 		abnormal aortic arch morphology J:105980
abnormal cardiac outflow tract development J:105980
abnormal craniofacial bone morphology J:109536
abnormal endolymphatic duct morphology J:109536
abnormal middle ear development J:109536
abnormal pharyngeal pouch morphology J:109536
abnormal vestibulocochlear ganglion morphology J:109536
absent cochlea J:109536
absent inner ear J:109536
absent inner ear vestibule J:109536
absent masseter muscle J:105980
absent middle ear ossicles J:105980, J:109536
absent outer ear J:105980, J:109536
absent parathyroid glands J:105980
absent pterygoid muscle J:105980
absent semicircular canals J:109536
absent tubotympanic recess J:109536
absent tympanic ring J:105980, J:109536
absent zygomatic arch J:105980
athymia J:105980
cleft secondary palate J:105980, J:109536
fusion of basioccipital and basisphenoid bone J:105980, J:109536
hyoid bone hypoplasia J:105980
inner ear hypoplasia J:109536
neonatal lethality, complete penetrance J:105980, J:109536
otic capsule hypoplasia J:109536
otic vesicle hypoplasia J:109536
persistent truncus arteriosus J:105980
pharynx hypoplasia J:105980
retroesophageal right subclavian artery J:105980
short mandible J:105980
skin edema J:105980
small otic vesicle J:109536
small thyroid gland J:105980
temporal bone hypoplasia J:105980
ventricular septal defect J:105980
Top2btm2Jcw/Top2btm2.1Jcw
Foxg1tm1(cre)Skm/Foxg1+
involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ 		abnormal cerebral cortex morphology J:94879
abnormal hippocampus granule cell layer J:94879
abnormal hippocampus morphology J:94879
abnormal hippocampus pyramidal cell layer J:94879
abnormal motor capabilities/coordination/movement J:94879
atelectasis J:94879
neonatal lethality, complete penetrance J:94879
respiratory failure J:94879
small olfactory bulb J:94879
Wnt9btm1Amc/Wnt9btm1Amc
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * 129X1/SvJ 		bilateral cleft upper lip J:178316
cleft palate J:178316
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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory