Mypn Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mypn
myopalladin
MGI:1916052

16 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mypn^em1(IMPC)J/Mypn^em1(IMPC)J C57BL/6NJ-Mypn^em1(IMPC)J/Mmjax	abnormal coat/hair pigmentation	J:211773
	abnormal vocalization	J:211773
	decreased leukocyte cell number	J:211773
Mypn^tm1.1Epu/Mypn⁺ either: (involves: 129S6/SvEv) or (involves: 129S6/SvEv * C57BL/6NCrl)	abnormal cardiac muscle relaxation	J:243710
	abnormal heart atrium morphology	J:243710
	abnormal heart echocardiography feature	J:243710
	abnormal heart left ventricle morphology	J:243710
	abnormal intercalated disk morphology	J:243710
	abnormal myocardial fiber morphology	J:243710
	abnormal T wave	J:243710
	atrioventricular block	J:243710
	cardiac interstitial fibrosis	J:243710
	irregular heartbeat	J:243710
Mypn^tm1.1Epu/Mypn^tm1.1Epu either: (involves: 129S6/SvEv) or (involves: 129S6/SvEv * C57BL/6NCrl)	no abnormal phenotype detected	J:243710
Mypn^tm1.1Epu/Mypn^tm1.1Epu involves: 129S6/SvEvTac	abnormal Z line morphology	J:248575
Mypn^tm1.1Epu/Mypn^tm1.1Epu involves: 129S6/SvEvTac	myopathy	J:248575

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 11/12/2024 MGI 6.24