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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Frs3
fibroblast growth factor receptor substrate 3
MGI:2135965
11 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
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+
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
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

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory