Mypn Phenotype Annotations

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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)
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