Phenotypes Associated with This Genotype

Genotype
MGI:5300249

• Allelic Composition: Prickle1^b2b019Clo/Prickle1^b2b019Clo
• Genetic Background: C57BL/6J-Prickle1^b2b019Clo

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

EFIC imaging reveals DORV and VSD

cardiovascular system

double outlet right ventricle, ventricular defect committed to aorta ( J:175213 )

perimembraneous ventricular septal defect ( J:175213 )

craniofacial

micrognathia ( J:175213 )

cleft palate ( J:175213 )

digestive/alimentary system

cleft palate ( J:175213 )

skeleton

micrognathia ( J:175213 )

growth/size/body

cleft palate ( J:175213 )

microcephaly ( J:175213 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
velocardiofacial syndrome		DOID:12583	OMIM:192430	J:175213