Phenotypes Associated with This Genotype

Genotype
MGI:5442135

• Allelic Composition: b2b1700Clo/b2b1700Clo
• Genetic Background: C57BL/6J-b2b1700Clo

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

Mutant 1700-007-LA displays situs inversus totalis indicated by mirror-image placement of the organs

cardiovascular system

vascular ring ( J:175213 )

double outlet right ventricle ( J:175213 )

d-loop transposition of the great arteries ( J:175213 )

atrial septal defect ( J:175213 )

dextrocardia ( J:175213 )

growth/size/body

heterotaxia ( J:175213 )

respiratory system

immotile respiratory cilia ( J:175213 )

digestive/alimentary system

abnormal digestive system morphology ( J:175213 )

• short gut

cellular

immotile respiratory cilia ( J:175213 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
Kartagener syndrome		DOID:0050144		J:175213
primary ciliary dyskinesia		DOID:9562	OMIM:PS244400	J:175213
visceral heterotaxy		DOID:0050545	OMIM:306955 OMIM:605376 OMIM:606325 OMIM:613751 OMIM:614779 OMIM:PS306955	J:175213