51 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lemd2em1(IMPC)Bay/Lemd2+ C57BL/6N-Lemd2em1(IMPC)Bay/Bay	abnormal eye posterior chamber depth	J:211773
	abnormal spleen morphology	J:211773
	decreased prepulse inhibition	J:211773
Lemd2em1(IMPC)Bay/Lemd2em1(IMPC)Bay C57BL/6N-Lemd2em1(IMPC)Bay/Bay	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Lemd2em1Eno/Lemd2em1Eno involves: C3H * C57BL/6 * C57BL/6N	abnormal heart echocardiography feature	J:331716
	abnormal heart electrocardiography waveform feature	J:331716
	abnormal heart morphology	J:331716
	abnormal myocardial fiber morphology	J:331716
	atrioventricular block	J:331716
	cardiac fibrosis	J:331716
	decreased cardiac muscle contractility	J:331716
	dilated cardiomyopathy	J:331716
	dilated heart atrium	J:331716
	dilated heart ventricle	J:331716
	increased myocardial fiber size	J:331716
	increased susceptibility to xenobiotic induced morbidity/mortality	J:331716
	normal muscle phenotype	J:331716
	premature death	J:331716
	prolonged PR interval	J:331716
	prolonged QRS complex duration	J:331716
	thin ventricular wall	J:331716
Lemd2em2Eno/Lemd2em2Eno Tg(Myh6-cre)2182Mds/0 involves: C3H * C57BL/6 * C57BL/6N * FVB/N	abnormal cardiovascular system physiology	J:331716
	abnormal heart echocardiography feature	J:331716
	abnormal heart morphology	J:331716
	abnormal myocardial fiber morphology	J:331716
	abnormal myocardial fiber physiology	J:331716
	decreased body size	J:331716
	dilated cardiomyopathy	J:331716
	dilated heart atrium	J:331716
	dilated heart ventricle	J:331716
	neonatal lethality, incomplete penetrance	J:331716
Lemd2Gt(DD0639)Wtsi/Lemd2+ B6.129P2-Lemd2Gt(DD0639)Wtsi	delayed skeletal muscle regeneration	J:221495
	normal muscle phenotype	J:221495
Lemd2Gt(DD0639)Wtsi/Lemd2Gt(DD0639)Wtsi B6.129P2-Lemd2Gt(DD0639)Wtsi	abnormal craniofacial development	J:221495
	abnormal dorsal root ganglion morphology	J:221495
	abnormal embryonic neuroepithelium morphology	J:221495
	abnormal embryonic tissue physiology	J:221495
	abnormal heart development	J:221495
	abnormal hindbrain morphology	J:221495
	abnormal mesenchyme morphology	J:221495
	abnormal midbrain morphology	J:221495
	abnormal retina neuronal layer morphology	J:221495
	abnormal somite development	J:221495
	absent embryonic telencephalon	J:221495
	anemia	J:221495
	decreased embryo size	J:221495
	decreased embryonic neuroepithelial cell proliferation	J:221495
	embryonic lethality during organogenesis, complete penetrance	J:221495
	impaired neuron differentiation	J:221495
	increased embryonic neuroepithelium apoptosis	J:221495
	intracranial hemorrhage	J:221495
	myocardial trabeculae hypoplasia	J:221495
	open neural tube	J:221495
	pale yolk sac	J:221495
	small pharyngeal arch	J:221495
	thin myocardium	J:221495