64 phenotypes from 6 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Disp1icb/Disp1icb involves: 129/Sv * C57BL/6J * SWR	abnormal brain development	J:94270
	abnormal facial morphology	J:94270
	abnormal heart development	J:94270
	abnormal limb morphology	J:94270
	abnormal somite development	J:94270
	abnormal vascular development	J:94270
	embryonic lethality, complete penetrance	J:94270
Disp1icb/Disp1icb involves: C3HeB/FeJ * C57BL/6J	abnormal direction of embryo turning	J:79027
	abnormal forelimb morphology	J:79027
	abnormal head shape	J:79027
	abnormal left-right axis patterning	J:98216
	abnormal neural tube morphology	J:79027
	abnormal spinal cord morphology	J:98216
	embryonic lethality during organogenesis, complete penetrance	J:79027, J:98216
	failure of heart looping	J:79027
	normal nervous system phenotype	J:79027
	pericardial edema	J:79027
Disp1icb/Disp1tm1Amc involves: 129X1/SvJ * C57BL/6J	abnormal basisphenoid bone morphology	J:92058
	abnormal craniofacial bone morphology	J:92058
	abnormal frontal bone morphology	J:92058
	abnormal head morphology	J:92058
	abnormal nasopharynx morphology	J:92058
	abnormal neurocranium morphology	J:92058
	abnormal occipital bone morphology	J:92058
	abnormal viscerocranium morphology	J:92058
	absent basisphenoid bone	J:92058
	absent occipital bone	J:92058
	absent parietal bone	J:92058
	absent pituitary gland	J:92058
	absent primary palate	J:92058
	absent upper incisors	J:92058
	absent vomeronasal organ	J:92058
	delayed chondrocyte differentiation	J:92058
	holoprosencephaly	J:92058
Disp1icb/Disp1tm1Amc Shhtm1(EGFP/cre)Cjt/Shh+ involves: 129X1/SvJ * C57BL/6J	oligodactyly	J:92504
Disp1icb/Disp1tm2Amc Shhtm1(EGFP/cre)Cjt/Shh+ involves: 129/Sv * C57BL/6J * SWR	abnormal facial morphology	J:94270
	abnormal nasal pit morphology	J:94270
	abnormal neuron differentiation	J:94270
	absent floor plate	J:94270
	absent parietal bone	J:94270
	absent premaxilla	J:94270
	neonatal lethality	J:94270
Disp1tm1Amc/Disp1tm1Amc involves: 129X1/SvJ	abnormal craniofacial bone morphology	J:92058
	abnormal facial morphology	J:92058
	abnormal nasopharynx morphology	J:92058
	abnormal neuron specification	J:92058
	abnormal vomeronasal organ morphology	J:92058
	absent primary palate	J:92058
	absent upper incisors	J:92058
	holoprosencephaly	J:92058
	neonatal lethality, complete penetrance	J:92058
	ocular hypotelorism	J:92058
	philtrum hypoplasia	J:92058
	pituitary gland hypoplasia	J:92058
	respiratory distress	J:92058
Disp1tm1Pab/Disp1tm1Pab involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal embryo turning	J:79457
	abnormal first pharyngeal arch morphology	J:79457
	abnormal heart looping	J:79457
	abnormal left-right axis patterning	J:79457
	abnormal neural fold formation	J:79457
	abnormal neural plate morphology	J:79457
	abnormal neural tube morphology	J:79457
	abnormal optic vesicle formation	J:79457
	abnormal somite development	J:79457
	decreased embryo size	J:79457
	distended pericardium	J:79457
	embryonic lethality during organogenesis, complete penetrance	J:79457
	fused first pharyngeal arch	J:79457
Disp1tm1Ptch/Disp1tm1Ptch involves: 129P2/OlaHsd	abnormal dermomyotome development	J:79831
	abnormal forebrain morphology	J:79831
	abnormal heart development	J:79831
	abnormal left-right axis symmetry of the somites	J:79831
	abnormal neural tube morphology	J:79831
	abnormal sclerotome morphology	J:79831
	absent floor plate	J:79831
	cyclopia	J:79831
	distended pericardium	J:79831
	embryonic lethality during organogenesis, complete penetrance	J:79831
	failure of heart looping	J:79831
	holoprosencephaly	J:79831
	incomplete embryo turning	J:79831
Disp1tm2.1Amc/Disp1tm2Amc Shhtm1(EGFP/cre)Cjt/Shh+ involves: 129/Sv * C57BL/6J * SWR	abnormal facial morphology	J:94270
	abnormal nasal pit morphology	J:94270
	abnormal neuron differentiation	J:94270
	abnormal parietal bone morphology	J:94270
	absent premaxilla	J:94270
	neonatal lethality	J:94270
Disp1tm2Amc/Disp1tm2Amc involves: 129/Sv * C57BL/6J * SWR	no abnormal phenotype detected	J:94270