26 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tdgtm1.1Abc/Tdgtm1.1Abc B6.129-Tdgtm1.1Abc	abnormal angiogenesis	J:174772
	abnormal cardiac outflow tract development	J:174772
	abnormal carotid artery morphology	J:174772
	abnormal coronary artery morphology	J:174772
	abnormal DNA methylation	J:174772
	abnormal dorsal aorta morphology	J:174772
	abnormal heart development	J:174772
	abnormal heart right ventricle morphology	J:174772
	abnormal limb development	J:174772
	abnormal mismatch repair	J:174772
	abnormal telencephalon development	J:174772
	abnormal vasculogenesis	J:174772
	embryonic growth arrest	J:174772
	embryonic lethality during organogenesis, complete penetrance	J:174772
	hemopericardium	J:174772
	hemorrhage	J:174772
	liver hemorrhage	J:174772
	myocardium hypoplasia	J:174772
	pericardial edema	J:174772
	pharyngeal arch hypoplasia	J:174772
	thin myocardium	J:174772
Tdgtm1Psch/Tdgtm1Psch involves: 129P2/OlaHsd * C57BL/6	embryonic lethality during organogenesis, complete penetrance	J:196259
	internal hemorrhage	J:196259
Tdgtm2.1Abc/Tdgtm2.1Abc B6.129-Tdgtm2.1Abc	abnormal DNA methylation	J:174772
	abnormal embryo turning	J:174772
	decreased embryo size	J:174772
	embryonic growth retardation	J:174772
	embryonic lethality during organogenesis, complete penetrance	J:174772
	pericardial effusion	J:174772
Tdgtm2Psch/Tdgtm2Psch involves: 129P2/OlaHsd * C57BL/6	embryonic lethality during organogenesis, complete penetrance	J:334509
	internal hemorrhage	J:334509