Ovol2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ovol2
ovo like zinc finger 2
MGI:1338039

49 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ovol2^tm1Sito/Ovol2^tm1Sito involves: 129P2/OlaHsd * C57BL/6J	abnormal angiogenesis	J:132526
	abnormal aortic sac morphology	J:132526
	abnormal blood circulation	J:132526
	abnormal embryonic tissue morphology	J:132526
	abnormal endocardium morphology	J:132526
	abnormal extraembryonic tissue morphology	J:132526
	abnormal heart development	J:132526
	abnormal heart looping	J:132526
	abnormal heart ventricle morphology	J:132526
	abnormal placenta vasculature	J:132526
	abnormal placental labyrinth vasculature morphology	J:132526
	abnormal vasculogenesis	J:132526
	abnormal vitelline vascular remodeling	J:132526
	abnormal vitelline vasculature morphology	J:132526
	absent intersomitic vessels	J:132526
	absent myocardial trabeculae	J:132526
	absent pharyngeal arches	J:132526
	absent vitelline blood vessels	J:132526
	decreased embryo size	J:132526
	embryonic growth retardation	J:132526
	embryonic lethality during organogenesis, complete penetrance	J:132526
	hemorrhage	J:132526
	open neural tube	J:132526
	small heart	J:132526
Ovol2^tm1Xdai/Ovol2^tm1Xdai either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	abnormal cephalic neural fold morphology	J:106405
	abnormal digestive system development	J:106405
	abnormal dorsal-ventral axis patterning	J:106405
	abnormal embryo turning	J:106405
	abnormal embryonic neuroepithelium morphology	J:106405
	abnormal forebrain development	J:106405
	abnormal foregut morphology	J:106405
	abnormal head mesenchyme morphology	J:106405
	abnormal heart development	J:106405
	abnormal heart looping	J:106405
	abnormal heart tube morphology	J:106405
	abnormal hindgut morphology	J:106405
	abnormal neural crest cell delamination	J:106405
	abnormal notochord morphology	J:106405
	abnormal optic eminence morphology	J:106405
	abnormal optic pit morphology	J:106405
	abnormal prechordal plate morphology	J:106405
	abnormal surface ectoderm morphology	J:106405
	absent otic pit	J:106405
	cardia bifida	J:106405
	common ventricle	J:106405
	decreased embryonic neuroepithelial cell proliferation	J:106405
	embryonic lethality during organogenesis, complete penetrance	J:106405
	incomplete rostral neuropore closure	J:106405
	increased embryonic neuroepithelium thickness	J:106405
	increased neural crest cell apoptosis	J:106405
	small pharyngeal arch	J:106405
	spina bifida	J:106405

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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