Phenotypes associated with this allele

• Allele Symbol: b2b386.1Clo
• Allele Name: Bench to Bassinet Program (B2B/CVDC), mutation 386.1 Cecilia Lo
• Allele ID: MGI:5605963
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	b2b386.1Clo/b2b386.1Clo	C57BL/6J-b2b386.1Clo	MGI:5605970

Genotype
MGI:5605970

hm1

• Allelic Composition: b2b386.1Clo/b2b386.1Clo
• Genetic Background: C57BL/6J-b2b386.1Clo

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

Mutant 386-005-1 presents with an anterior aorta which is diagnosed as DORV by EFIC imaging

cardiovascular system

coronary fistula ( J:175213 )

abnormal inferior vena cava morphology ( J:175213 )

• dual/bilateral inferior vena cava (IVC)

myocardial hypertrabeculation ( J:175213 )

• Excessive myocardial trabeculation or noncompaction

double outlet right ventricle ( J:175213 )

double outlet right ventricle with atrioventricular septal defect ( J:175213 )

common atrium ( J:175213 )

atrioventricular septal defect ( J:175213 )

ventricular septal defect ( J:175213 )

respiratory system

left pulmonary isomerism ( J:175213 )

• Left bronchial isomerism

muscle

myocardial hypertrabeculation ( J:175213 )

• Excessive myocardial trabeculation or noncompaction

hematopoietic system

absent spleen ( J:175213 )

immune system

absent spleen ( J:175213 )

growth/size/body

heterotaxia ( J:175213 )

abdominal situs ambiguus ( J:175213 )

left pulmonary isomerism ( J:175213 )

• Left bronchial isomerism

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