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Phenotypes Associated with This Genotype
Genotype
MGI:4949907
Allelic
Composition
Adgra2tm1.2Bstc/Adgra2tm1.2Bstc
Genetic
Background
B6.Cg-Adgra2tm1.2Bstc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Adgra2tm1.2Bstc mutation (0 available); any Adgra2 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• some mice are born alive but die within hours of birth
• mice are either stillborn or die within hours of birth with all dead by P0.5
• expected numbers are found from E9.5 to E17.5

cardiovascular system
• glomeruloid bodies are found in the ventral aspect of the spinal cord
• however, vessels appear normal in the midbrain, hindbrain, dorsal spinal cord, and non nervous system tissues
• in the pallium vessels form abnormal "glomeruloid-like" bodies adjacent to the perineural vascular plexus
• glomeruloids are detected in the ganglionic eminence as early as E10.5
• at E10.5 vessel sprouting resembles sprouting in wild-type mice at E9.5
• at E11.5 vessel sprouts form small glomeruloids that increase in size with age
• endothelial stalks connect the glomeruliods to the perineural vascular plexus
• glomeruloid structures are typically composed of multiple tufted vascular channels
• however, vessels formed normally along the longitudinal cerebral fissure
• at E10.5 vessel sprouting in the pallium resembles sprouting in wild-type mice at E9.5
• increases in severity during development
• seen in most mice
• at E17.5 bleeding into the outer wall of the telencephalic vesicles with intraventricular blood leakage and enlarged, distorted, lateral ventricles
• common but with variable severity
• occasionally seen in the absence of intracranial hemorrhage
• following intracardiac injection, biotin is found in intra- and extravascular regions in the forebrain
• however, no difference in permeability is seen in non-CNS vessels
• following intracardiac injection, biotin is found in intra- and extravascular regions in the ventral spinal cord

nervous system
• in the pallium vessels form abnormal "glomeruloid-like" bodies adjacent to the perineural vascular plexus
• glomeruloids are detected in the ganglionic eminence as early as E10.5
• at E10.5 vessel sprouting resembles sprouting in wild-type mice at E9.5
• at E11.5 vessel sprouts form small glomeruloids that increase in size with age
• endothelial stalks connect the glomeruliods to the perineural vascular plexus
• glomeruloid structures are typically composed of multiple tufted vascular channels
• however, vessels formed normally along the longitudinal cerebral fissure
• increases in severity during development
• seen in most mice
• at E17.5 bleeding into the outer wall of the telencephalic vesicles with intraventricular blood leakage and enlarged, distorted, lateral ventricles
• common but with variable severity
• occasionally seen in the absence of intracranial hemorrhage
• following intracardiac injection, biotin is found in intra- and extravascular regions in the forebrain
• however, no difference in permeability is seen in non-CNS vessels
• following intracardiac injection, biotin is found in intra- and extravascular regions in the ventral spinal cord
• increases in severity during development
• loose packing of neuroepithelial cells with large open spaces in tissue surrounding glomeruloid bodies
• occasional breaks between cortical marginal glia are present
• at E15.5 a marked failure of neocortex development is seen
• notably thinner at E13.5
• at E17.5 bleeding into the outer wall of the telencephalic vesicles (pallium) with intraventricular blood leakage and enlarged, distorted, lateral ventricles


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
04/16/2024
MGI 6.23
The Jackson Laboratory