25 phenotypes from 3 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Thap11em1Poche/Thap11em1Poche C57BL/6J-Thap11em1Poche	abnormal astrocyte morphology	J:317822
	abnormal craniofacial development	J:317822
	abnormal craniofacial morphology	J:317822
	abnormal enzyme/coenzyme activity	J:317822
	abnormal enzyme/coenzyme level	J:317822
	abnormal trabecula carnea morphology	J:317822
	abnormal ventricle myocardium morphology	J:317822
	cyanosis	J:317822
	decreased embryo size	J:317822
	decreased erythrocyte cell number	J:317822
	decreased hematocrit	J:317822
	decreased hemoglobin content	J:317822
	enlarged lateral ventricles	J:317822
	exencephaly	J:317822
	kinked tail	J:317822
	neonatal lethality, complete penetrance	J:317822
	respiratory failure	J:317822
	thin cerebral cortex	J:317822
	thrombocytopenia	J:317822
	vertebral transformation	J:317822
Thap11tm1.1Tpz/Thap11tm1.1Tpz involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal cell physiology	J:136306
	absent inner cell mass proliferation	J:136306
	embryonic lethality between implantation and somite formation, complete penetrance	J:136306
Thap11tm1Tpz/Thap11em1Poche E2f1Tg(Wnt1-cre)2Sor/E2f1+ involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	belly spot	J:317822
	decreased digit pigmentation	J:317822
Thap11tm1Tpz/Thap11tm1Tpz involves: 129S1/Sv * 129X1/SvJ	abnormal cell physiology	J:136306
Thap11tm1Tpz/Thap11tm1Tpz E2f1Tg(Wnt1-cre)2Sor/E2f1+ involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C3H * C57BL/6	abnormal craniofacial development	J:317822
Thap11tm1Tpz/Thap11tm1Tpz Tg(Prrx1-cre)1Cjt/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J	abnormal craniofacial development	J:317822