36 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Del(6Dlx6-Dlx5)1Tlu/+ Mef2ctm1Eno/Mef2c+ involves: 129S7/SvEvBrd	abnormal palate development	J:122483
	cyanosis	J:122483
	glossoptosis	J:122483
	neonatal lethality, complete penetrance	J:122483
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Mef2ctm1Eno/Mef2ctm1Jjs H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S4/SvJaeSor * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J * CBA/J	normal embryo phenotype	J:122483
Hdac4tm1Eno/Hdac4tm1Eno Mef2ctm1Eno/Mef2c+ involves: 129S7/SvEvBrd	normal skeleton phenotype	J:119152
Ighg1tm1(cre)Cgn/0 Mef2btm1.1Rdf/Mef2btm1.1Rdf Mef2ctm2Eno/Mef2ctm2Eno involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	decreased germinal center B cell number	J:265465
Mef2atm1.1Limm/Mef2atm1.1Limm Mef2ctm1Jjs/Mef2ctm1Jjs Tg(Cdh5-cre/ERT2)1Rha/0 involves: 129S/SvEv * 129S6/SvEvTac	abnormal retina vasculature morphology	J:334208
	decreased angiogenesis	J:334208
Mef2atm1.1Limm/Mef2atm1.1Limm Mef2ctm2Eno/Mef2ctm2Eno Mef2dtm3Eno/Mef2dtm3Eno Tg(GFAP-cre)25Mes/0 involves: 129S/SvEv * C57BL/6 * FVB/N	abnormal long-term potentiation	J:207812
	decreased body weight	J:207812
	decreased brain size	J:207812
	enhanced paired-pulse facilitation	J:207812
	increased neuron apoptosis	J:207812
	normal nervous system phenotype	J:207812
	premature death	J:207812
Mef2ctm1.1Wtp/Mef2ctm1.1Wtp involves: 129S4/SvJae * C57BL/6 * SJL * Swiss Webster	perinatal lethality	J:185868
Mef2ctm1Eno/Mef2c+ Mef2dtm1.1Eno/Mef2d+ involves: 129S7/SvEvBrd	failure of sternum ossification	J:119152
	neonatal lethality, complete penetrance	J:119152
Mef2ctm1Jjs/Mef2ctm1Jjs Mir223tm1Fcam/Mir223tm1Fcam Lyz2tm1(cre)Ifo/Lyz2+ involves: 129 * C57BL/6	abnormal neutrophil differentiation	J:140009
	abnormal neutrophil physiology	J:140009
	increased neutrophil cell number	J:140009
Mef2ctm2Eno/Mef2ctm2Eno Mef2dtm1Eno/Mef2dtm1Eno Tg(Col2a1-cre)1Bhr/0 involves: 129S/SvEv * C57BL/6 * SJL	failure of endochondral bone ossification	J:119152
Tg(Col2a1-Mef2c/VP16)1Eno/0 Not Specified	abnormal epiphyseal plate morphology	J:119152
	abnormal forelimb morphology	J:119152
	abnormal neurocranium morphology	J:119152
	premature endochondral bone ossification	J:119152
	short limbs	J:119152
Tg(Myh6-Mef2c)2Jmol/0 involves: FVB	abnormal heart atrium morphology	J:111573
	cardiac hypertrophy	J:111573
	decreased cardiac muscle contractility	J:111573
	dilated cardiomyopathy	J:111573
	dilated heart left ventricle	J:111573
	dilated heart ventricle	J:111573
	increased heart ventricle size	J:111573
Tg(Myh6-Mef2c)2Jmol/0 Tg(Myh6-Ppp3ca)37Eno/0 involves: FVB	abnormal heart atrium morphology	J:111573
	cardiac hypertrophy	J:111573
	decreased cardiac muscle contractility	J:111573
Tg(Myh6-Mef2c/VP16)1Eno/0 Not Specified	abnormal skeletal muscle fiber type ratio	J:127416
	enhanced exercise endurance	J:127416