Foxp2 Phenotype Annotations - Multigenic Genotypes

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Foxp1^tm1Eem/Foxp1⁺ Foxp2^tm1Bux/Foxp2^tm1Bux 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
Foxp1^tm1Eem/Foxp1^tm1Eem Foxp2^tm1Bux/Foxp2^tm1Bux involves: 129X1/SvJ * C57BL/6	decreased embryo size	J:121421
	embryonic lethality, complete penetrance	J:121421
Foxp2^tm1Woen/Foxp2^tm1Woen 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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