56 phenotypes from 5 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lyz2tm1(cre)Ifo/Lyz2+ Pdcd10tm1Wami/Pdcd10tm1Wami involves: 129 * 129P2/OlaHsd * C57BL/6	abnormal neutrophil morphology	J:256076
	abnormal neutrophil physiology	J:256076
	increased circulating creatinine level	J:256076
	renal tubular necrosis	J:256076
Pdcd10tm1.1Kwhi/Pdcd10tm1.1Kwhi involves: C57BL/6	embryonic growth arrest	J:173947
	embryonic lethality between somite formation and embryo turning, complete penetrance	J:173947
Pdcd10tm1.1Wami/Pdcd10tm1.1Wami involves: 129 * C57BL/6	abnormal vasculogenesis	J:171969
	anemia	J:171969
	decreased embryo size	J:171969
	embryonic lethality between somite formation and embryo turning, incomplete penetrance	J:171969
	embryonic lethality during organogenesis, complete penetrance	J:171969
	impaired hematopoiesis	J:171969
	myocardial trabeculae hypoplasia	J:171969
	pallor	J:171969
	thin myocardium	J:171969
Pdcd10tm1Arte/Pdcd10tm1Arte Tg(Cdh5-cre/ERT2)1Rha/0 involves: C57BL/6	abnormal brain vasculature morphology	J:177584
	abnormal retina vasculature morphology	J:177584
Pdcd10tm1Kwhi/Pdcd10tm1.1Kwhi Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/? involves: C57BL/6 * CBA	abnormal astrocyte morphology	J:173947
	abnormal brain vasculature morphology	J:173947
	abnormal pericyte morphology	J:173947
	CNS inflammation	J:173947
	postnatal lethality	J:173947
Pdcd10tm1Kwhi/Pdcd10tm1Kwhi Nfatc1tm1.1(cre)Bz/Nfatc1+ involves: 129S1/Sv * 129X1/SvJ	abnormal cardiac jelly morphology	J:238897
	lethality throughout fetal growth and development, complete penetrance	J:238897
	thin myocardium	J:238897
Pdcd10tm1Kwhi/Pdcd10tm1Kwhi Tg(Nes-cre)1Kln/? involves: C57BL/6 * SJL	no abnormal phenotype detected	J:173947
Pdcd10tm1Kwhi/Pdcd10tm1Kwhi Tg(Tek-cre)1Ywa/? involves: C57BL/6 * SJL	abnormal cardinal vein morphology	J:173947
	normal cardiovascular system phenotype	J:173947
	embryonic lethality during organogenesis, complete penetrance	J:173947
Pdcd10tm1Wami/Pdcd10tm1Wami Emx1tm1(cre)Krj/Emx1+ involves: 129 * 129S2/SvPas * C57BL/6	abnormal brain vasculature morphology	J:170480
	astrocytosis	J:170480
	increased brain size	J:170480
	increased hemangioma incidence	J:170480
	normal mortality/aging	J:170480
Pdcd10tm1Wami/Pdcd10tm1Wami Taglntm2(cre)Yec/Tagln+ involves: 129 * 129S6/SvEvTac * C57BL/6	normal cardiovascular system phenotype	J:171969
	normal mortality/aging	J:171969
Pdcd10tm1Wami/Pdcd10tm1Wami Tg(GFAP-cre)25Mes/0 involves: 129 * C57BL/6 * FVB/N	abnormal brain morphology	J:170480
	abnormal brain vasculature morphology	J:170480
	abnormal gait	J:170480
	abnormal vascular endothelial cell migration	J:170480
	astrocytosis	J:170480
	circling	J:170480
	decreased body weight	J:170480
	dilated brain ventricle	J:170480
	dilated vasculature	J:170480
	hydrocephaly	J:170480
	increased brain size	J:170480
	increased hemangioma incidence	J:170480
	postnatal growth retardation	J:170480
	postnatal lethality, incomplete penetrance	J:170480
	premature death	J:170480
Pdcd10tm1Wami/Pdcd10tm1Wami Tg(Nes-cre)1Kln/0 involves: 129 * C57BL/6 * SJL	abnormal brain morphology	J:170480
	increased brain size	J:170480
	normal mortality/aging	J:171969
	postnatal lethality, complete penetrance	J:170480
	prenatal lethality, incomplete penetrance	J:170480
Pdcd10tm1Wami/Pdcd10tm1Wami Tg(Tek-cre)12Flv/0 involves: 129 * C3H * C57BL/6	abnormal angiogenesis	J:171969
	abnormal brain vasculature morphology	J:171969
	abnormal cardinal vein morphology	J:171969
	abnormal developmental vascular remodeling	J:171969
	abnormal dorsal aorta morphology	J:171969
	abnormal endocardium morphology	J:171969
	abnormal intersomitic vessel morphology	J:171969
	abnormal myocardium layer morphology	J:171969
	abnormal vascular branching morphogenesis	J:171969
	abnormal vitelline vascular remodeling	J:171969
	abnormal vitelline vasculature morphology	J:171969
	anemia	J:171969
	dilated dorsal aorta	J:171969
	embryonic lethality during organogenesis, complete penetrance	J:171969
	enlarged pericardium	J:171969
	impaired hematopoiesis	J:171969
	microcephaly	J:171969
	myocardial trabeculae hypoplasia	J:171969
	normal nervous system phenotype	J:171969
	pallor	J:171969
	thin myocardium	J:171969