About   Help   FAQ
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 morphology 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory