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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gbx2
gastrulation brain homeobox 2
MGI:95668
75 phenotypes from 5 alleles in 9 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
En1tm2(cre)Wrst/En1+
Gbx2tm1.1Mrt/Gbx2tm1.1Alj
involves: 129/Sv * C57BL/6 * SJL * Swiss Webster
abnormal cerebellar foliation J:79431
abnormal cerebellum development J:79431
abnormal midbrain development J:79431
abnormal midbrain-hindbrain boundary morphology J:79431
abnormal postnatal growth J:79431
cerebellum vermis hypoplasia J:79431
decreased body weight J:79431
decreased embryonic neuroepithelial cell proliferation J:79431
decreased embryonic neuroepithelium thickness J:79431
increased inferior colliculus size J:79431
normal mortality/aging J:79431
normal nervous system phenotype J:79431
postnatal lethality, incomplete penetrance J:79431
Gbx2tm1.1(cre/ERT2)Jyhl/Gbx2tm1.1Mrt
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL
absent cerebellum J:147282
Gbx2tm1.1Alj/Gbx2tm1.1Alj
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6
no abnormal phenotype detected J:79431
Gbx2tm1.1Mrt/Gbx2tm1.1Alj
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * SJL
no abnormal phenotype detected J:79431
Gbx2tm1.1Mrt/Gbx2tm1.1Mrt
B6.129-Gbx2tm1.1Mrt
abnormal aortic arch morphology J:100584
abnormal cardiovascular system morphology J:100584
abnormal cerebellum morphology J:100584
abnormal fourth pharyngeal arch artery morphology J:100584
abnormal innervation J:100584
abnormal neural crest cell migration J:100584
abnormal neural crest cell morphology J:100584
abnormal styloid process morphology J:100584
abnormal trigeminal ganglion morphology J:100584
abnormal vascular endothelial cell differentiation J:100584
absent trigeminal nerve J:100584
cleft palate J:100584
cyanosis J:100584
decreased neural crest cell number J:100584
double outlet right ventricle J:100584
fusion of glossopharyngeal and vagus nerve J:100584
fusion of middle ear ossicles J:100584
interrupted aortic arch, type b J:100584
middle ear ossicle hypoplasia J:100584
neonatal lethality, complete penetrance J:100584
otic capsule hypoplasia J:100584
overriding aortic valve J:100584
perimembraneous ventricular septal defect J:100584
retroesophageal right subclavian artery J:100584
right aortic arch J:100584
styloid process hypoplasia J:100584
Gbx2tm1.1Mrt/Gbx2tm1.1Mrt
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J) or (involves: 129S1/Sv * 129X1/SvJ * FVB/N)
abnormal cerebellum development J:42110
abnormal choroid plexus morphology J:42110
abnormal forebrain development J:42110
abnormal hindbrain morphology J:42110
abnormal inferior colliculus morphology J:42110
abnormal locus ceruleus morphology J:42110
abnormal membranous labyrinth morphology J:42110
abnormal metencephalon morphology J:42110
abnormal midbrain development J:42110
abnormal midbrain morphology J:42110
abnormal midbrain-hindbrain boundary development J:42110
abnormal midbrain-hindbrain boundary morphology J:42110
abnormal motor neuron morphology J:42110
abnormal pons morphology J:42110
absent cerebellum J:42110
absent supraoccipital bone J:42110
neonatal lethality, complete penetrance J:42110
small otic vesicle J:42110
Gbx2tm1.1Mrt/Gbx2tm1.1Mrt
involves: 129S1/Sv * 129X1/SvJ * Swiss Webster
abnormal cochlear ganglion morphology J:98487
abnormal cochlear sensory epithelium morphology J:98487
abnormal crista ampullaris morphology J:98487
abnormal hindbrain development J:98487
abnormal inner ear morphology J:98487
abnormal membranous labyrinth morphology J:98487
abnormal metencephalon morphology J:98487
abnormal organ of Corti morphology J:98487
abnormal rhombomere 5 morphology J:98487
abnormal vestibular saccular macula morphology J:98487
absent cochlear ganglion J:98487
absent common crus J:98487
absent endolymphatic duct J:98487
absent lateral semicircular canal J:98487
absent posterior semicircular canal J:98487
absent scala media J:98487
absent superior semicircular canal J:98487
absent vestibular saccule J:98487
decreased cochlea coiling J:98487
inner ear cyst J:98487
small otic vesicle J:98487
Gbx2tm1.1Mrt/Gbx2tm1.2Alj
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ
abnormal cardiovascular system morphology J:79431
abnormal nervous system morphology J:79431
abnormal skeleton morphology J:79431
preweaning lethality, complete penetrance J:79431
Gbx2tm1Mrt/Gbx2+
Tg(Nes-cre)1Atp/?
involves: 129S1/Sv * 129X1/SvJ * FVB/N
no abnormal phenotype detected J:111945

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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