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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Rbfox2
RNA binding protein, fox-1 homolog (C. elegans) 2
MGI:1933973
46 phenotypes from 1 allele in 3 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Rbfox2tm1.1Dblk/Rbfox2tm1.1Dblk
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: 129S2/SvPas * 129S4/SvJae * C57BL/6J 		abnormal craniofacial bone morphology J:279139
abnormal frontal bone morphology J:279139
abnormal nasal bone morphology J:279139
abnormal palatal mesenchymal cell proliferation J:279139
absent palatine bone horizontal plate J:279139
normal cardiovascular system phenotype J:279139
cleft secondary palate J:279139
decreased bone ossification J:279139
normal endocrine/exocrine gland phenotype J:279139
frontal bone hypoplasia J:279139
neonatal lethality, complete penetrance J:279139
palatal shelves fail to meet at midline J:279139
normal skeleton phenotype J:279139
small mandible J:279139
Rbfox2tm1.1Dblk/Rbfox2tm1.1Dblk
Pax3tm1(cre)Joe/0
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J 		abnormal axial skeleton morphology J:279139
abnormal craniofacial bone morphology J:279139
abnormal craniofacial morphology J:279139
abnormal frontal bone morphology J:279139
abnormal hypoglossal nerve morphology J:279139
abnormal nasal bone morphology J:279139
abnormal neurocranium morphology J:279139
abnormal oculomotor nerve morphology J:279139
abnormal palatal mesenchymal cell proliferation J:279139
abnormal rostral-caudal body axis extension J:279139
abnormal spine curvature J:279139
abnormal trochlear nerve morphology J:279139
absent palatine bone horizontal plate J:279139
atelectasis J:279139
normal cardiovascular system phenotype J:279139
cleft secondary palate J:279139
decreased bone ossification J:279139
ectopic bone J:279139
normal endocrine/exocrine gland phenotype J:279139
frontal bone hypoplasia J:279139
fusion of vertebral bodies J:279139
normal muscle phenotype J:279139
neonatal lethality, complete penetrance J:279139
palatal shelves fail to meet at midline J:279139
respiratory distress J:279139
respiratory failure J:279139
small mandible J:279139
small thoracic cavity J:279139
subcutaneous edema J:279139
thin dermal layer J:279139
Rbfox2tm1.1Dblk/Rbfox2tm1.1Dblk
Tg(Nes-cre)1Kln/0
involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL 		abnormal locomotor activation J:181631
abnormal neuron physiology J:181631
abnormal posture J:181631
abnormal Purkinje cell migration J:181631
normal behavior/neurological phenotype J:176189
decreased body weight J:181631
decreased cerebellar granule cell precursor proliferation J:181631
ectopic Purkinje cell J:181631
hydrocephaly J:181631
increased neuron apoptosis J:181631
increased Purkinje cell number J:181631
lethality, incomplete penetrance J:181631
postnatal lethality, incomplete penetrance J:181631
small cerebellum J:181631
thin cerebellar molecular layer J:181631
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