Foxd2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Foxd2
forkhead box D2
MGI:1347471

11 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Foxd2^{em1(IMPC)Hmgu}/Foxd2⁺ C57BL/6NCrl-Foxd2^{em1(IMPC)Hmgu}/Ieg	abnormal optic disk morphology	J:211773
	abnormal retina morphology	J:211773
	decreased grip strength	J:211773
Foxd2^{em1(IMPC)Hmgu}/Foxd2^{em1(IMPC)Hmgu} C57BL/6NCrl-Foxd2^{em1(IMPC)Hmgu}/Ieg	abnormal optic disk morphology	J:211773
	decreased locomotor activity	J:211773
	decreased vertical activity	J:211773
	hyperactivity	J:211773
	short tibia	J:211773
Foxd2^tm1Blh/Foxd2^tm1Blh involves: 129S6/SvEvTac * Black Swiss	hydronephrosis	J:60219
	hydroureter	J:60219
	short ureter	J:60219
	small kidney	J:60219
Foxd2^tm1Blh/Foxd2^tm1Blh involves: 129S6/SvEvTac * C57BL/6	hydronephrosis	J:60219
	hydroureter	J:60219
	short ureter	J:60219
	small kidney	J:60219

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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