41 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Gata4tm1.1Jmol/Gata4tm1.1Jmol Tg(Myh6-Map2k1*)1Jmol/0 involves: 129 * C57BL/6 * FVB	abnormal heart size	J:174537
Gata4tm1.1Sad/Gata4tm1.1Sad Tg(Myh6-Map2k1*)1Jmol/0 involves: 129S1/Sv * 129X1/SvJ * FVB	cardiac hypertrophy	J:174537
Gata4tm1.1Sad/Gata4tm1.1Sad Tg(Myh6-Map2k1*)1Jmol/0 Tg(Myh7-cre)1Jmk/0 involves: 129S1/Sv * 129X1/SvJ * FVB	abnormal heart size	J:174537
Hivep3tm3Glm/Hivep3+ Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Tg(Prrx1-cre)1Cjt/0 involves: 129 * C57BL/6J * SJL * SJL/J	increased bone mass	J:201597
Krastm1Bbd/Kras+ Map2k1tm1Chrn/Map2k1tm1Chrn involves: 129S1/Sv * 129X1/SvJ	increased lung non-small cell carcinoma incidence	J:172200
	premature death	J:172200
Krastm1Bbd/Kras+ Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL	decreased classified tumor incidence	J:172200
	premature death	J:172200
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129/Sv * C57BL/6J * CBA/J * SJL	abnormal eye distance/ position	J:144862
	abnormal outer ear morphology	J:144862
	absent tongue	J:144862
	mandible hypoplasia	J:144862
	persistent truncus arteriosus	J:144862
	short maxilla	J:144862
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd involves: 129/Sv * C57BL/6J * SJL	abnormal crypts of Lieberkuhn morphology	J:172200
	abnormal intestine morphology	J:172200
	premature death	J:172200
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Tg(Cyp17a1-icre)AJako/0 involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	abnormal circulating androgen level	J:278979
	abnormal testosterone level	J:278979
	decreased copulatory plug deposition	J:278979
	decreased Leydig cell number	J:278979
	decreased litter size	J:278979
	decreased seminal vesicle weight	J:278979
	decreased testes secretion	J:278979
	increased circulating luteinizing hormone level	J:278979
	reduced male fertility	J:278979
	normal reproductive system phenotype	J:278979
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Tg(KRT14-cre)1Efu/? involves: 129/Sv * C57BL/6J * SJL	abnormal outer ear morphology	J:122484
	abnormal tongue epithelium morphology	J:122484
	abnormal vibrissa follicle morphology	J:122484
	decreased body size	J:122484
	decreased body weight	J:122484
	decreased hair follicle cell proliferation	J:122484
	decreased hair follicle number	J:122484
	eyelids open at birth	J:122484
	impaired skin barrier function	J:122484
	increased keratinocyte apoptosis	J:122484
	neonatal lethality, incomplete penetrance	J:122484
	shiny skin	J:122484
	skin hypoplasia	J:122484
	translucent skin	J:122484
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Tg(KRT14-cre/ERT2)1Ipc/? involves: 129/Sv * C57BL/6J * SJL	abnormal tongue epithelium morphology	J:122484
	skin hypoplasia	J:122484
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Tg(KRT14-RAF1/ESR1)1Pkha/? involves: 129/Sv * C57BL/6 * C57BL/6J * SJL	skin hypoplasia	J:122484
Mapk1tm1Melo/Mapk1+ Tg(Myh6-Map2k1*)1Jmol/0 involves: 129S2/SvPas * FVB	cardiac hypertrophy	J:124903
Mapk3tm1Gpg/Mapk3tm1Gpg Tg(Myh6-Map2k1*)1Jmol/0 involves: 129/Sv * FVB/N	cardiac hypertrophy	J:124903
Tg(Myh6-Map2k1*)1Jmol/0 Tg(Myh6/tetO-Tnnc1*I61Q)1Jmol/0 Tg(Myh6-tTA)55Rbns/0 involves: FVB	abnormal heart left ventricle morphology	J:234490
	increased cardiac muscle contractility	J:234490
	increased heart weight	J:234490
	thick interventricular septum	J:234490