Qrich1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Qrich1
glutamine-rich 1
MGI:1916482

15 phenotypes from 4 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Qrich1^b2b2404Clo/Qrich1^b2b2404Clo C57BL/6J-Qrich1^b2b2404Clo	abnormal myocardium compact layer morphology	J:175213
	cleft palate	J:175213
	double outlet right ventricle	J:175213
	double outlet right ventricle with atrioventricular septal defect	J:175213
	overriding aortic valve	J:175213
	perimembraneous ventricular septal defect	J:175213
	polycystic kidney	J:175213
	thymus hypoplasia	J:175213
	ventricular septal defect	J:175213
Qrich1^em1Nki/Qrich1^em1Nki involves: C57BL/6JRj	no abnormal phenotype detected	J:369749
Qrich1^em2Nki/Qrich1^em2Nki involves: C57BL/6JRj	decreased mean corpuscular hemoglobin	J:369749
	embryonic lethality during organogenesis, incomplete penetrance	J:369749
	increased embryonic neuroepithelium apoptosis	J:369749
	prenatal lethality, complete penetrance	J:369749
	thin placenta labyrinth	J:369749
Qrich1^em3Nki/Qrich1^em3Nki involves: C57BL/6JRj	decreased mean corpuscular hemoglobin	J:369749
	embryonic lethality during organogenesis, incomplete penetrance	J:369749
	increased embryonic neuroepithelium apoptosis	J:369749
	prenatal lethality, complete penetrance	J:369749
	thin placenta labyrinth	J:369749

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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