29 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ighg1tm1(cre)Cgn/0 Mef2dtm3Eno/Mef2dtm3Eno involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	normal hematopoietic system phenotype	J:265465
Mef2dtm1.2Tfur/Mef2dtm1.2Tfur involves: 129S6/SvEvTac * C57BL/6 * SJL	abnormal electroretinogram waveform feature	J:230346
	abnormal retina bipolar cell morphology	J:230346
	abnormal retina cone bipolar cell morphology	J:230346
	abnormal retina horizontal cell morphology	J:230346
	abnormal retina outer nuclear layer morphology	J:230346
	abnormal retina outer plexiform layer morphology	J:230346
	decreased a-wave amplitude	J:230346
	decreased b-wave amplitude	J:230346
	decreased retina cone cell number	J:230346
	decreased retina rod cell number	J:230346
	retina outer nuclear layer degeneration	J:230346
	retina photoreceptor degeneration	J:230346
	short photoreceptor outer segment	J:230346
	short retina cone cell outer segment	J:230346
	short retina rod cell outer segment	J:230346
	thin retina outer nuclear layer	J:230346
	normal vision/eye phenotype	J:230346
Mef2dtm1Eno/Mef2dtm1Eno Tg(Myog-cre)1Eno/0 Not Specified	abnormal skeletal muscle fiber type ratio	J:127416
Mef2dtm3Eno/Mef2dtm3Eno Meox2tm1(cre)Sor/Meox2+ involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * SJL	abnormal heart morphology	J:130825
	abnormal heart size	J:130825
	abnormal myocardial fiber morphology	J:130825
	decreased cardiac muscle contractility	J:130825
Tg(Myh6-Mef2d)2Eno/0 Not Specified	abnormal thrombosis	J:130825
	cardiac fibrosis	J:130825
	cardiomyopathy	J:130825
	increased heart atrium size	J:130825
	liver vascular congestion	J:130825
	pulmonary vascular congestion	J:130825