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Symbol
Name
ID

Nxn
nucleoredoxin
MGI:109331

Phenotype annotations related to cardiovascular system

Darker colors indicate more annotations

Mouse Phenotypes		absent stapedial artery	abnormal retina blood vessel morphology	dilated liver sinusoidal space	abnormal vitelline vein topology	persistent truncus arteriosus	double outlet right ventricle	atrioventricular septal defect	perimembraneous ventricular septal defect	ventricular septal defect	decreased cardiac muscle contractility
Availability	Mouse Genotype	absent stapedial artery	abnormal retina blood vessel morphology	dilated liver sinusoidal space	abnormal vitelline vein topology	persistent truncus arteriosus	double outlet right ventricle	atrioventricular septal defect	perimembraneous ventricular septal defect	ventricular septal defect	decreased cardiac muscle contractility
	Nxn^{tm1b(EUCOMM)Wtsi}/Nxn^{tm1b(EUCOMM)Wtsi}
	Nxn^tm1Hmik/Nxn^tm1Hmik
	Nxn^em1(IMPC)Bay/Nxn⁺
	Nxn^{tm1a(EUCOMM)Wtsi}/Nxn⁺

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23