51 phenotypes from 5 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Has2tm1.1Chg/Has2tm1.1Chg H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	abnormal mandible morphology	J:283393
	abnormal maxilla morphology	J:283393
	abnormal Meckel's cartilage morphology	J:283393
	abnormal oral cavity morphology	J:283393
	abnormal palate development	J:283393
	complete cleft palate	J:283393
	decreased palatal shelf size	J:283393
	failure of palatal shelf elevation	J:283393
	increased tongue size	J:283393
	micrognathia	J:283393
	neonatal lethality, complete penetrance	J:283393
	protruding tongue	J:283393
	short mandible	J:283393
	short Meckel's cartilage	J:283393
Has2tm1.1Chg/Has2tm1.2Chg Tg(Hoxb6-cre)#Mku/0 involves: 129 * Black Swiss * C57BL/6 * FVB/N * SJL	abnormal cartilage development	J:194283
	abnormal cartilage morphology	J:194283
	abnormal chondrocyte differentiation	J:194283
	abnormal digit morphology	J:194283
	abnormal joint morphology	J:194283
	abnormal limb mesenchyme morphology	J:194283
Has2tm1.1Nita/Has2tm1.1Nita B6.129-Has2tm1.1Nita	no abnormal phenotype detected	J:164205
Has2tm1.1Yama/Has2tm1.1Yama Tg(Prrx1-cre)1Cjt/0 involves: 129X1/SvJ * C57BL/6 * FVB/N * SJL/J	abnormal cartilage morphology	J:152912
	abnormal chondrocyte morphology	J:152912
	abnormal digit development	J:152912
	abnormal gait	J:152912
	abnormal joint morphology	J:152912
	abnormal limb development	J:152912
	abnormal long bone epiphyseal ossification zone morphology	J:152912
	abnormal long bone epiphyseal plate morphology	J:152912
	abnormal phalanx morphology	J:152912
	decreased chondrocyte number	J:152912
	disorganized long bone epiphyseal plate	J:152912
	short limbs	J:152912
Has2tm1Jam/Has2tm1Jam involves: 129P2/OlaHsd * C57BL/6J	abnormal blood vessel morphology	J:63748
	abnormal cardiac epithelial to mesenchymal transition	J:63748
	abnormal cardiac outflow tract development	J:63748
	abnormal embryonic tissue morphology	J:63748
	abnormal extraembryonic endoderm formation	J:63748
	abnormal head mesenchyme morphology	J:63748
	abnormal heart morphology	J:63748
	abnormal somite shape	J:63748
	abnormal visceral yolk sac morphology	J:63748
	absent atrioventricular cushions	J:63748
	absent cardiac jelly	J:63748
	absent trabeculae carneae	J:63748
	absent vitelline blood vessels	J:63748
	decreased heart right ventricle size	J:63748
	embryonic growth retardation	J:63748
	embryonic lethality during organogenesis, complete penetrance	J:63748
	heart atrium hypoplasia	J:63748
	incomplete embryo turning	J:63748
	irregular heartbeat	J:63748
	pericardial edema	J:63748