Nos1ap Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Nos1ap
nitric oxide synthase 1 (neuronal) adaptor protein
MGI:1917979

19 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nos1ap^{tm1b(KOMP)Wtsi}/Nos1ap⁺ C57BL/6N-Nos1ap^{tm1b(KOMP)Wtsi}/Bay	tremors	J:211773
Nos1ap^{tm1b(KOMP)Wtsi}/Nos1ap^{tm1b(KOMP)Wtsi} C57BL/6N-Nos1ap^{tm1b(KOMP)Wtsi}/Bay	abnormal optic disk morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal urinary bladder morphology	J:211773
	decreased bone mineral content	J:211773
	decreased circulating alanine transaminase level	J:211773
	hyperactivity	J:211773
	increased vertical activity	J:211773
Nos1ap^tm1Tsso/Nos1ap^tm1Tsso involves: C57BL/6JJcl	abnormal action potential	J:268528
	normal cardiovascular system phenotype	J:268528
	decreased cardiac muscle contractility	J:268528
	increased susceptibility to xenobiotic induced morbidity/mortality	J:268528
	irregular heartbeat	J:268528
	oxidative stress	J:268528
	prolonged QRS complex duration	J:268528
	prolonged QT interval	J:268528
	ventricular fibrillation	J:268528
	ventricular premature beat	J:268528
	ventricular tachycardia	J:268528

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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