30 phenotypes from 6 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rtel1tm1.1Hdin/Rtel1tm1.1Hdin involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL	abnormal neural tube morphology	J:130490
	abnormal placenta morphology	J:130490
	embryonic lethality during organogenesis, complete penetrance	J:130490
	enlarged allantois	J:130490
	pericardial effusion	J:130490
Rtel1tm1Hdin/Rtel1tm1Hdin involves: 129S1/Sv * 129X1/SvJ	decreased DNA replication	J:202812
Rtel1tm1Hdin/Rtel1tm1Hdin involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	no abnormal phenotype detected	J:130490
Rtel1tm1Pml/Rtel1tm1Pml involves: 129S1/Sv * 129X1/SvJ	abnormal cell differentiation	J:91351
	abnormal cephalic neural fold morphology	J:91351
	abnormal dermomyotome development	J:91351
	abnormal head paraxial mesoderm morphology	J:91351
	abnormal heart ventricle morphology	J:91351
	abnormal myotome development	J:91351
	abnormal neural crest cell morphology	J:91351
	abnormal neural tube morphology	J:91351
	abnormal placenta vasculature	J:91351
	decreased embryo size	J:91351
	decreased trophoblast giant cell number	J:91351
	embryonic growth retardation	J:91351
	embryonic lethality during organogenesis, complete penetrance	J:91351
	enlarged floor plate	J:91351
	failure of chorioallantoic fusion	J:91351
	hematoma	J:91351
	hemopericardium	J:91351
	incomplete rostral neuropore closure	J:91351
	small allantois	J:91351
	small ectoplacental cone	J:91351
Rtel1tm2.1Hdin/Rtel1tm2.1Hdin involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal cell physiology	J:202812
	abnormal mitosis	J:202812
	abnormal telomere morphology	J:202812
	normal cellular phenotype	J:202812
	decreased DNA replication	J:202812
	early cellular replicative senescence	J:202812
Rtel1tm2.1Pml/Rtel1tm2.1Pml 129.129P2(B6)-Rtel1tm2.1Pml	no abnormal phenotype detected	J:197762
Rtel1tm3.1Hdin/Rtel1tm3.1Hdin involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal cellular phenotype	J:202812