Tead2 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tead2
TEA domain family member 2
MGI:104904

29 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Sox11^tm2.2Weg/Sox11⁺ Sox4^tm1.1Vlf/Sox4⁺ Tead2^tm1Hssk/Tead2^tm1Hssk involves: 129 * C57BL/6 * CBA * FVB/N	abnormal notochord morphology	J:175338
	abnormal vertebrae morphology	J:175338
	double outlet right ventricle	J:175338
	ventricular septal defect	J:175338
Tead1^tm1Hssk/Tead1⁺ Tead2^tm1Hssk/Tead2^tm1Hssk either: (involves: C57BL/6 * CBA) or (involves: C57BL/6 * CBA * CD-1)	exencephaly	J:131426
	incomplete rostral neuropore closure	J:131426
Tead1^tm1Hssk/Tead1⁺ Tead2^tm1Hssk/Tead2^tm1Hssk Yap1^tm1Smil/Yap1⁺ either: (involves: 129S/SvEv * C57BL/6 * CBA) or (involves: 129S/SvEv * C57BL/6 * CBA * CD-1)	abnormal developmental patterning	J:131426
	abnormal embryo turning	J:131426
Tead1^tm1Hssk/Tead1^tm1Hssk Tead2^tm1Hssk/Tead2⁺ either: (involves: C57BL/6 * CBA) or (involves: C57BL/6 * CBA * CD-1)	embryonic growth retardation	J:131426
Tead1^tm1Hssk/Tead1^tm1Hssk Tead2^tm1Hssk/Tead2⁺ Yap1^tm1Smil/Yap1⁺ either: (involves: 129S/SvEv * C57BL/6 * CBA) or (involves: 129S/SvEv * C57BL/6 * CBA * CD-1)	abnormal allantois morphology	J:131426
	abnormal embryo development	J:131426
	abnormal embryonic tissue morphology	J:131426
Tead1^tm1Hssk/Tead1^tm1Hssk Tead2^tm1Hssk/Tead2^tm1Hssk either: (involves: C57BL/6 * CBA) or (involves: C57BL/6 * CBA * CD-1)	abnormal allantois morphology	J:131426
	abnormal developmental patterning	J:131426
	abnormal embryonic tissue morphology	J:131426
	abnormal extraembryonic tissue morphology	J:131426
	abnormal heart tube morphology	J:131426
	abnormal lateral plate mesoderm morphology	J:131426
	abnormal neural plate morphology	J:131426
	abnormal notochord morphology	J:131426
	abnormal paraxial mesoderm morphology	J:131426
	abnormal posterior definitive endoderm morphology	J:131426
	abnormal vitelline vasculature morphology	J:131426
	absent notochord	J:131426
	absent somites	J:131426
	decreased cell proliferation	J:131426
	decreased embryo size	J:131426
	disorganized embryonic tissue	J:131426
	embryonic lethality during organogenesis, complete penetrance	J:131426
	failure of chorioallantoic fusion	J:131426
	failure of initiation of embryo turning	J:131426
	increased embryonic tissue cell apoptosis	J:131426
	open neural tube	J:131426

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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