Phenotypes Associated with This Genotype

Genotype
MGI:7279300

• Allelic Composition: Glyr1^em1Dsr/Glyr1^em1Dsr
• Genetic Background: involves: C57BL/6J

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

mortality/aging

postnatal lethality, incomplete penetrance ( J:322763 )

• 54% newborns die by age P1

cardiovascular system

ventricular septal defect ( J:322763 )

• VSD in 15% of newborns

embryo

embryo phenotype ( J:322763 )

N • born at normal Mendelian ratios

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
atrioventricular septal defect		DOID:0050651	OMIM:606215 OMIM:614430 OMIM:614474	J:322763