Phenotypes associated with this allele

• Allele Symbol: Odad2^b2b227.1Clo
• Allele Name: Bench to Bassinet Program (B2B/CVDC), mutation 227, subline 1 Cecilia Lo
• Allele ID: MGI:5437099
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Odad2^b2b227.1Clo/Odad2^b2b227.1Clo	C57BL/6J-Odad2^b2b227.1Clo	MGI:5437109

Genotype
MGI:5437109

hm1

• Allelic Composition: Odad2^b2b227.1Clo/Odad2^b2b227.1Clo
• Genetic Background: C57BL/6J-Odad2^b2b227.1Clo

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

Mutant 227-002-NC exhibits dextrocardia with duplicated inferior vena cava (IVC) and parallel outflow tracts which is diagnosed as DORV by EFIC imaging

cardiovascular system

double outlet right ventricle ( J:175213 )

dextrocardia ( J:175213 )

mesocardia ( J:175213 )

ventricular septal defect ( J:175213 )

cardiomyopathy ( J:175213 )

digestive/alimentary system

right-sided stomach ( J:175213 )

growth/size/body

lung cyst ( J:175213 )

heterotaxia ( J:175213 )

right-sided stomach ( J:175213 )

situs inversus totalis ( J:175213 )

hematopoietic system

spleen hypoplasia ( J:175213 )

immune system

spleen hypoplasia ( J:175213 )

muscle

cardiomyopathy ( J:175213 )

respiratory system

abnormal respiratory motile cilium physiology ( J:175213 )

• dyskinetic cilia

immotile respiratory cilia ( J:175213 )

lung cyst ( J:175213 )

abnormal respiration ( J:175213 )

cellular

abnormal respiratory motile cilium physiology ( J:175213 )

• dyskinetic cilia

immotile respiratory cilia ( J:175213 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
primary ciliary dyskinesia 23		DOID:0110609	OMIM:615451	J:175213
visceral heterotaxy		DOID:0050545	OMIM:306955 OMIM:605376 OMIM:606325 OMIM:613751 OMIM:614779 OMIM:PS306955	J:175213