Phenotypes associated with this allele

• Allele Symbol: b2b2815Clo
• Allele Name: Bench to Bassinet Program (B2B/CVDC), mutation 2815 Cecilia Lo
• Allele ID: MGI:5616525
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	b2b2815Clo/b2b2815Clo	C57BL/6J-b2b2815Clo	MGI:5616526

Genotype
MGI:5616526

hm1

• Allelic Composition: b2b2815Clo/b2b2815Clo
• Genetic Background: C57BL/6J-b2b2815Clo

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

Mutant (E15.5) presents with parallel outflow tracts which was diagnosed as overriding aorta by ECM imaging

cardiovascular system

overriding aortic valve ( J:175213 )

perimembraneous ventricular septal defect ( J:175213 )

cardiac hypertrophy ( J:175213 )

• ventricular hypertrophy

craniofacial

absent mandible ( J:175213 )

micrognathia ( J:175213 )

cleft palate ( J:175213 )

short snout ( J:175213 )

lowered ear position ( J:175213 )

skeleton

absent mandible ( J:175213 )

micrognathia ( J:175213 )

vision/eye

anophthalmia ( J:175213 )

digestive/alimentary system

cleft palate ( J:175213 )

growth/size/body

cardiac hypertrophy ( J:175213 )

• ventricular hypertrophy

cleft palate ( J:175213 )

short snout ( J:175213 )

lowered ear position ( J:175213 )

hearing/vestibular/ear

lowered ear position ( J:175213 )

renal/urinary system

abnormal kidney morphology ( J:175213 )

• multiplex kidneys