47 phenotypes from 3 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Dph1tm1.1Cmch/Dph1tm1.1Cmch Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA	abnormal tongue position	J:214744
	absent palatine bone	J:214744
	cleft palate	J:214744
	edema	J:214744
	fetal growth retardation	J:214744
	mandible hypoplasia	J:214744
	neonatal lethality, complete penetrance	J:214744
	palatal shelves fail to meet at midline	J:214744
	pallor	J:214744
	short mandible	J:214744
	small cranium	J:214744
Dph1tm1.1Cmch/Dph1tm1.1Cmch H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	cleft palate	J:214744
	decreased cranium length	J:214744
	postnatal lethality, incomplete penetrance	J:214744
	round face	J:214744
	short mandible	J:214744
	short Meckel's cartilage	J:214744
	short nasal bone	J:214744
Dph1tm1.1Cmch/Dph1tm1.1Cmch Mesp1tm2(cre)Ysa/Mesp1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	normal craniofacial phenotype	J:214744
	postnatal lethality, incomplete penetrance	J:214744
Dph1tm1Bhr/Dph1+ involves: 129/Sv * C57BL/6	increased tumor incidence	J:88090
Dph1tm1Bhr/Dph1tm1Bhr either: 129/Sv or (involves: 129/Sv * C57BL/6)	abnormal cell cycle	J:88090
	abnormal craniofacial bone morphology	J:88090
	abnormal lung development	J:88090
	abnormal neural tube morphology	J:88090
	abnormal skeleton development	J:88090
	cleft palate	J:88090
	decreased fetal weight	J:88090
	embryonic growth retardation	J:88090
	embryonic lethality during organogenesis, incomplete penetrance	J:88090
	embryonic lethality, complete penetrance	J:88090
	hydrops fetalis	J:88090
	increased nucleated erythrocyte cell number	J:88090
	neonatal lethality, complete penetrance	J:88090
	preaxial polydactyly	J:88090
	primary atelectasis	J:88090
	respiratory failure	J:88090
	thick lung-associated mesenchyme	J:88090
Dph1tm1Bhr/Dph1tm1Bhr involves: 129S4/SvJae	abnormal cell physiology	J:188600
	decreased fibroblast proliferation	J:188600
	decreased sensitivity to induced cell death	J:188600
Dph1tm1Bhr/Dph1tm2Bhr involves: 129/Sv * C57BL/6	decreased fetal weight	J:88090
	embryonic growth retardation	J:88090
	embryonic lethality during organogenesis, incomplete penetrance	J:88090
	hydrops fetalis	J:88090
	neonatal lethality, complete penetrance	J:88090
Dph1tm2Bhr/Dph1+ involves: 129/Sv * C57BL/6	increased tumor incidence	J:88090
Dph1tm2Bhr/Dph1tm2Bhr either: 129/Sv or (involves: 129/Sv * C57BL/6)	abnormal cell cycle	J:88090
	abnormal craniofacial bone morphology	J:88090
	abnormal embryo turning	J:88090
	abnormal eye morphology	J:88090
	abnormal eye pigmentation	J:88090
	abnormal hepatoblast morphology	J:88090
	abnormal lung development	J:88090
	abnormal neural tube morphology	J:88090
	abnormal skeleton development	J:88090
	abnormal somite development	J:88090
	cleft palate	J:88090
	decreased fetal weight	J:88090
	embryonic growth retardation	J:88090
	embryonic lethality during organogenesis, incomplete penetrance	J:88090
	embryonic lethality, complete penetrance	J:88090
	hydrops fetalis	J:88090
	increased nucleated erythrocyte cell number	J:88090
	liver degeneration	J:88090
	neonatal lethality, complete penetrance	J:88090
	preaxial polydactyly	J:88090
	primary atelectasis	J:88090
	respiratory failure	J:88090
	thick lung-associated mesenchyme	J:88090
Dph1tm2Bhr/Dph1tm2Bhr involves: 129S4/SvJae * C57BL/6J	abnormal tongue position	J:214744
	absent palatine bone	J:214744
	cleft secondary palate	J:214744
	decreased body size	J:214744
	decreased palatal shelf size	J:214744
	lethality at weaning, complete penetrance	J:214744
	micrognathia	J:214744
	palatal shelves fail to meet at midline	J:214744
	preaxial polydactyly	J:214744
	short Meckel's cartilage	J:214744
	small cranium	J:214744