Foxn4 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Foxn4
forkhead box N4
MGI:2151057

19 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Foxn4^{em1(IMPC)Ccpcz}/Foxn4⁺ C57BL/6NCrl-Foxn4^{em1(IMPC)Ccpcz}/Ccpcz	abnormal cranium morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal tooth color	J:211773
	decreased lean body mass	J:211773
	decreased prepulse inhibition	J:211773
	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	J:211773
	increased freezing behavior	J:211773
	increased total body fat amount	J:211773
Foxn4^{em1(IMPC)Ccpcz}/Foxn4^{em1(IMPC)Ccpcz} C57BL/6NCrl-Foxn4^{em1(IMPC)Ccpcz}/Ccpcz	no spontaneous movement	J:211773
Foxn4^tm1Xia/Foxn4^tm1Xia involves: 129S6/SvEvTac * C57BL/6J	abnormal retina ganglion cell morphology	J:92622
	abnormal retina neuronal layer morphology	J:92622
	absent retina horizontal cells	J:92622
	decreased amacrine cell number	J:92622
	increased retina apoptosis	J:92622
	increased retina photoreceptor cell number	J:92622
	postnatal lethality, incomplete penetrance	J:92622
	retina hypoplasia	J:92622

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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