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Phenotypes Associated with This Genotype
Genotype
MGI:3839105
Allelic
Composition
Megf8hlb611/Megf8hlb611
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Megf8hlb611 mutation (0 available); any Megf8 mutation (96 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Left-right asymmetric defects in Megf8hlb611/Megf8hlb611 embryos

cardiovascular system
• the outflow tract is shortened compared to in wild-type mice
• 100% of E13.5-E14.5 mutants exhibit transposition of the great arteries (J:311933)
• mice exhibit abnormal pulmonary venous connections
• 67% of E13.5-E14.5 mutants exhibit abnormal cardiac apex; mesocardiac or dextrocardia
• in some mice (J:146805)
• in some mice (J:146805)
• 100% of E13.5-E14.5 mutants exhibit cardiac septum defects, either ventricular septal defect or atrioventricular septal defect

limbs/digits/tail
• 100% of E13.5-E14.5 mutants exhibit preaxial digit duplication

hematopoietic system
N
• erythropoiesis is normal
• in some mice
• in some mice

embryo
N
• despite heterotaxia, mice exhibit normal nodal cilia rotation

digestive/alimentary system
• right-sided stomach

respiratory system
• 92% of E13.5-E14.5 mutants exhibit abnormal lung situs

growth/size/body
• 100% of of E13.5-E14.5 mutants exhibit heterotaxy and situs inversus (J:311933)
• right-sided stomach
• 67% of E13.5-E14.5 mutants exhibit abnormal abdomen situs
• 92% of E13.5-E14.5 mutants exhibit abnormal lung situs
• 100% of of E13.5-E14.5 mutants exhibit heterotaxy and situs inversus

immune system
• in some mice
• in some mice


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory