Phenotypes associated with this allele

• Allele Symbol: Megf8^b2b288Clo
• Allele Name: Bench to Bassinet Program (B2B/CVDC), mutation 288 Cecilia Lo
• Allele ID: MGI:5311364
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Megf8^b2b288Clo/Megf8^b2b288Clo	C57BL/6J-Megf8^b2b288Clo	MGI:5311833

Genotype
MGI:5311833

hm1

• Allelic Composition: Megf8^b2b288Clo/Megf8^b2b288Clo
• Genetic Background: C57BL/6J-Megf8^b2b288Clo

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

Dextrocardia

cardiovascular system

double outlet right ventricle, ventricular defect committed to aorta ( J:175213 )

• (DORV;{ILL})

d-loop transposition of the great arteries ( J:175213 )

• (TGA;{SDD})

dextrocardia ( J:175213 )

complete atrioventricular septal defect ( J:175213 )

• Complete common atrioventricular canal

growth/size/body

cleft palate ( J:175213 )

short snout ( J:175213 )

heterotaxia ( J:175213 )

craniofacial

micrognathia ( J:175213 )

cleft palate ( J:175213 )

short snout ( J:175213 )

digestive/alimentary system

cleft palate ( J:175213 )

vision/eye

anophthalmia ( J:175213 )

skeleton

micrognathia ( J:175213 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
Carpenter syndrome		DOID:0060234	OMIM:201000 OMIM:614976	J:175213
visceral heterotaxy		DOID:0050545	OMIM:306955 OMIM:605376 OMIM:606325 OMIM:613751 OMIM:614779 OMIM:PS306955	J:175213