23 phenotypes from 5 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Senp2Gt(AN0727)Wtsi/Senp2Gt(AN0727)Wtsi involves: 129P2/OlaHsd	abnormal atrioventricular cushion morphology	J:162938
	abnormal cardiac epithelial to mesenchymal transition	J:162938
	abnormal heart development	J:162938
	embryonic lethality during organogenesis, complete penetrance	J:162938
	pericardial effusion	J:162938
	thin myocardium	J:162938
Senp2Gt(OST66117)Lex/Senp2+ B6;129S5-Senp2Gt(OST66117)Lex/Orl	decreased circulating glucose level	J:82809
Senp2Gt(OST66117)Lex/Senp2Gt(OST66117)Lex B6;129S5-Senp2Gt(OST66117)Lex/Orl	prenatal lethality, complete penetrance	J:82809
Senp2tm1.1Eyeh/Senp2tm1.1Eyeh A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ involves: FVB/N	normal mortality/aging	J:217910
	normal nervous system phenotype	J:217910
Senp2tm1Eyeh/Senp2tm1Eyeh Not Specified	abnormal brain wave pattern	J:217910
	abnormal nervous system electrophysiology	J:217910
	abnormal neuron physiology	J:217910
	atrioventricular block	J:217910
	audiogenic seizures	J:217910
	convulsive seizures	J:217910
	premature death	J:217910
	sinus bradycardia	J:217910
Senp2tm1Whsu/Senp2tm1Whsu involves: 129S6/SvEvTac * C57BL/6	abnormal trophoblast giant cell morphology	J:144707
	abnormal trophoblast layer morphology	J:144707
	absent trophoblast giant cells	J:144707
	decreased spongiotrophoblast size	J:144707
	embryonic lethality during organogenesis, complete penetrance	J:144707
	small placenta	J:144707