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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Foxp2
forkhead box P2
MGI:2148705
16 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Foxp1tm1Eem/Foxp1+
Foxp2tm1Bux/Foxp2tm1Bux
involves: 129X1/SvJ * C57BL/6
abnormal branching involved in lung morphogenesis J:121421
abnormal esophageal smooth muscle morphology J:121421
abnormal esophagus development J:121421
abnormal lung development J:121421
decreased lung weight J:121421
decreased mesenchymal cell proliferation involved in lung development J:121421
dilated esophagus J:121421
dilated respiratory conducting tube J:121421
perinatal lethality, complete penetrance J:121421
small lung J:121421
Foxp1tm1Eem/Foxp1tm1Eem
Foxp2tm1Bux/Foxp2tm1Bux
involves: 129X1/SvJ * C57BL/6
decreased embryo size J:121421
embryonic lethality, complete penetrance J:121421
Foxp2tm1Woen/Foxp2tm1Woen
involves: C57BL/6 * C57BL/6J
decreased exploration in new environment J:150425
decreased locomotor activity J:150425
decreased QRS amplitude J:150425
decreased vocalization J:150425

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
04/16/2024
MGI 6.23
The Jackson Laboratory