Foxp4 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Foxp4
forkhead box P4
MGI:1921373

13 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Foxp4^{Gt(RRF116)Byg}/Foxp4^{Gt(RRF116)Byg} involves: 129P2/OlaHsd	abnormal floor plate morphology	J:188384
	abnormal neural tube morphology	J:188384
	abnormal notochord morphology	J:188384
	embryonic lethality during organogenesis, incomplete penetrance	J:188384
	exencephaly	J:188384
	holoprosencephaly	J:188384
	spina bifida	J:188384
Foxp4^{Gt(RRF116)Byg}/Foxp4^tm1Eem involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	abnormal neural tube morphology	J:188384
Foxp4^tm1Eem/Foxp4^tm1Eem involves: 129S1/Sv * 129X1/SvJ	abnormal neural tube morphology	J:188384
Foxp4^tm1Eem/Foxp4^tm1Eem involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal cardiovascular system physiology	J:92817
	abnormal digestive system development	J:92817
	abnormal heart morphology	J:92817
	abnormal heart position or orientation	J:92817
	cardia bifida	J:92817
	embryonic lethality during organogenesis, incomplete penetrance	J:92817
	tracheoesophageal fistula	J:92817

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 09/08/2026 MGI 6.24