Phenotypes associated with this allele

• Allele Symbol: b2b2739Clo
• Allele Name: Bench to Bassinet Program (B2B/CVDC), mutation 2739 Cecilia Lo
• Allele ID: MGI:5560910
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	b2b2739Clo/b2b2739Clo	C57BL/6J-b2b2739Clo	MGI:5561552

Genotype
MGI:5561552

hm1

• Allelic Composition: b2b2739Clo/b2b2739Clo
• Genetic Background: C57BL/6J-b2b2739Clo

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

Mutant 2739-005-1 (E15.5) shows abnormal arrangement of the great arteries and thin ventricular walls which is diagnosed as DORV and ventricular non-compaction by EFIC imaging

cardiovascular system

abnormal aortic arch morphology ( J:175213 )

right aortic arch ( J:175213 )

vascular ring ( J:175213 )

abnormal left subclavian artery morphology ( J:175213 )

abnormal myocardium compact layer morphology ( J:175213 )

• Excessive myocardial trabeculation or noncompaction

double outlet right ventricle ( J:175213 )

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

double outlet right ventricle, Taussig bing type ( J:175213 )

atrioventricular septal defect ( J:175213 )

ventricular septal defect ( J:175213 )

craniofacial

micrognathia ( J:175213 )

cleft upper lip ( J:175213 )

cleft palate ( J:175213 )

digestive/alimentary system

cleft palate ( J:175213 )

growth/size/body

cleft upper lip ( J:175213 )

cleft palate ( J:175213 )

decreased body size ( J:175213 )

integument

petechiae ( J:175213 )

skeleton

micrognathia ( J:175213 )

vision/eye

microphthalmia ( J:175213 )

anophthalmia ( J:175213 )

muscle

abnormal myocardium compact layer morphology ( J:175213 )

• Excessive myocardial trabeculation or noncompaction