88 phenotypes from 8 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Prickle1b2b019Clo/Prickle1b2b019Clo C57BL/6J-Prickle1b2b019Clo	cleft palate	J:175213
	double outlet right ventricle, ventricular defect committed to aorta	J:175213
	microcephaly	J:175213
	micrognathia	J:175213
	perimembraneous ventricular septal defect	J:175213
Prickle1em1Yzou/Prickle1+ C57BL/6-Prickle1em1Yzou	abnormal excitatory synapse morphology	J:321396
	abnormal social investigation	J:321396
	abnormal spatial reference memory	J:321396
	increased susceptibility to pharmacologically induced seizures	J:321396
Prickle1em1Yzou/Prickle1em1Yzou C57BL/6-Prickle1em1Yzou	abnormal excitatory synapse morphology	J:321396
	abnormal object recognition memory	J:321396
	abnormal social investigation	J:321396
Prickle1m1Ingm/Prickle1+ involves: C57BL/6	abnormal seizure response to electrical stimulation	J:169136
Prickle1m1Ingm/Prickle1m1Ingm involves: C57BL/6	normal mortality/aging	J:169136
Prickle1m2Ingm/Prickle1+ C57BL/6-Prickle1m2Ingm	abnormal seizure response to electrical stimulation	J:169136
Prickle1m2Ingm/Prickle1m2Ingm C57BL/6-Prickle1m2Ingm	abnormal palatal mesenchymal cell proliferation	J:223183
	abnormal palatal rugae morphology	J:223183
	abnormal palatal shelf morphology	J:223183
	abnormal secondary palate development	J:223183
	cleft secondary palate	J:223183
	decreased maxillary shelf size	J:223183
	decreased palatal shelf size	J:223183
	failure of palatal shelf elevation	J:223183
	palatal shelves fail to meet at midline	J:223183
	prenatal lethality, complete penetrance	J:169136
	short snout	J:223183
Prickle1tm1.2Asw/Prickle1tm1.2Asw Not Specified	abnormal chondrocyte morphology	J:213772
	abnormal cochlear hair cell stereociliary bundle morphology	J:213772
	abnormal developmental patterning	J:213772
	abnormal digit morphology	J:213772
	abnormal fetal cardiomyocyte morphology	J:213772
	abnormal hair follicle morphology	J:213772
	abnormal hair follicle orientation	J:213772
	abnormal hippocampus morphology	J:213772
	abnormal innervation	J:213772
	abnormal kidney collecting duct morphology	J:213772
	abnormal kidney morphology	J:213772
	abnormal myocardial fiber morphology	J:213772
	abnormal nervous system tract morphology	J:213772
	abnormal nose morphology	J:213772
	abnormal phalanx morphology	J:213772
	abnormal proximal convoluted tubule morphology	J:213772
	abnormal renal tubule morphology	J:213772
	abnormal striatum morphology	J:213772
	abnormal ureteric bud morphology	J:213772
	atrial septal defect	J:213772
	bifid tongue	J:213772
	cleft palate	J:213772
	decreased body size	J:213772
	decreased length of long bones	J:213772
	delayed endochondral bone ossification	J:213772
	delayed neural tube closure	J:213772
	dilated renal tubule	J:213772
	embryonic lethality during organogenesis, incomplete penetrance	J:213772
	enlarged lateral ventricles	J:213772
	eyelids open at birth	J:213772
	increased diameter of long bones	J:213772
	increased heart right atrium size	J:213772
	kidney cyst	J:213772
	misaligned sternebrae	J:213772
	postnatal lethality, complete penetrance	J:213772
	short cochlear hair cell stereocilia	J:213772
	short forelimb	J:213772
	short limbs	J:213772
	short mandible	J:213772
	short nasal bone	J:213772
	short premaxilla	J:213772
	short snout	J:213772
	short tail	J:213772
	short tongue	J:213772
	transposition of great arteries	J:213772
	wavy tail	J:213772
Prickle1tm1.2Asw/Prickle1tm1.3Asw Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: C57BL/6 * CBA	abnormal hair follicle development	J:213772
	abnormal hair follicle orientation	J:213772
Prickle1tm1.3Asw/Prickle1tm1.3Asw Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: C57BL/6 * CBA	postnatal lethality, complete penetrance	J:213772
Prickle1tm1Asw/Prickle1tm1.2Asw Not Specified	abnormal eyelid cilium morphology	J:213772
	abnormal eyelid morphology	J:213772
	abnormal vertebrae development	J:213772
	brachydactyly	J:213772
	decreased body length	J:213772
	decreased length of long bones	J:213772
	flattened snout	J:213772
	fused lower incisors	J:213772
	kinked tail	J:213772
	ocular hypertelorism	J:213772
	prominent forehead	J:213772
	short snout	J:213772
Prickle1tm1Asw/Prickle1tm1Asw Not Specified	abnormal eyelid cilium morphology	J:213772
	abnormal eyelid morphology	J:213772
	abnormal vertebrae development	J:213772
	brachydactyly	J:213772
	decreased body length	J:213772
	decreased length of long bones	J:213772
	flattened snout	J:213772
	fused lower incisors	J:213772
	ocular hypertelorism	J:213772
	prominent forehead	J:213772
	short snout	J:213772
Prickle1tm1Nue/Prickle1+ B6.Cg-Prickle1tm1Nue	abnormal seizure response to electrical stimulation	J:169136
Prickle1tm1Nue/Prickle1tm1Nue involves: C57BL/6 * CBA	abnormal anterior visceral endoderm cell migration	J:151993
	abnormal embryonic epiblast morphology	J:151993
	abnormal extraembryonic endoderm formation	J:151993
	abnormal mitotic spindle morphology	J:151993
	absent mesoderm	J:151993
	decreased mitotic index	J:151993
	embryonic growth arrest	J:151993
	embryonic lethality between somite formation and embryo turning, complete penetrance	J:151993
	failure of primitive streak formation	J:151993
	increased embryonic tissue cell apoptosis	J:151993