Phenotypes associated with this allele

• Allele Symbol: Myh10^b2b2437Clo
• Allele Name: Bench to Bassinet Program (B2B/CVDC), mutation 2437 Cecilia Lo
• Allele ID: MGI:5552947
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myh10^b2b2437Clo/Myh10^b2b2437Clo	C57BL/6J-Myh10^b2b2437Clo	MGI:5554178

Genotype
MGI:5554178

hm1

• Allelic Composition: Myh10^b2b2437Clo/Myh10^b2b2437Clo
• Genetic Background: C57BL/6J-Myh10^b2b2437Clo

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

Mutant 2437-005-3 (E16.5) exhibits parallel outflow tracts and is diagnosed with DORV and ventricular non-compaction by EFIC imaging

cardiovascular system

abnormal myocardium compact layer morphology ( J:175213 )

• ventricular myocardial non-compaction

double outlet right ventricle ( J:175213 )

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

overriding aortic valve ( J:175213 )

atrioventricular septal defect ( J:175213 )

ventricular septal defect ( J:175213 )

craniofacial

abnormal cranium morphology ( J:175213 )

micrognathia ( J:175213 )

cleft upper lip ( J:175213 )

nervous system

exencephaly ( J:175213 )

skeleton

abnormal cranium morphology ( J:175213 )

micrognathia ( J:175213 )

growth/size/body

cleft upper lip ( J:175213 )

muscle

abnormal myocardium compact layer morphology ( J:175213 )

• ventricular myocardial non-compaction