33 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc31a1tm1Djt/Slc31a1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal copper level	J:69897
	decreased liver iron level	J:69897
Slc31a1tm1Djt/Slc31a1tm1Djt involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal embryonic neuroepithelium morphology	J:69897
	abnormal mesenchyme morphology	J:69897
	abnormal mesoderm development	J:69897
	decreased embryo size	J:69897
	delayed neural tube closure	J:69897
	embryonic lethality during organogenesis, complete penetrance	J:69897
	failure of initiation of embryo turning	J:69897
Slc31a1tm1Jgt/Slc31a1+ involves: 129X1/SvJ * C57BL/6	decreased brain copper level	J:69862
	prenatal lethality, incomplete penetrance	J:69862
Slc31a1tm1Jgt/Slc31a1tm1Jgt involves: 129X1/SvJ * C57BL/6	abnormal basement membrane morphology	J:69862
	abnormal embryonic tissue morphology	J:69862
	abnormal Reichert's membrane morphology	J:69862
	absent allantois	J:69862
	absent mesoderm	J:69862
	decreased Reichert's membrane thickness	J:69862
	embryonic lethality during organogenesis, complete penetrance	J:69862
	hemorrhage	J:69862
	thin endoderm	J:69862
Slc31a1tm2Djt/Slc31a1tm2Djt Tg(Vil1-cre)997Gum/0 involves: 129 * C57BL/6 * FVB/N * SJL	abnormal copper level	J:129741
	abnormal heart morphology	J:129741
	abnormal liver copper level	J:129741
	ataxia	J:129741
	decreased body weight	J:129741
	decreased circulating copper level	J:129741
	decreased spleen weight	J:129741
	enlarged heart	J:129741
	hemosiderosis	J:129741
	hypopigmentation	J:129741
	kinked vibrissae	J:129741
	loose skin	J:129741
	postnatal growth retardation	J:129741
	postnatal lethality, incomplete penetrance	J:129741
	weight loss	J:129741