Myl7 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myl7
myosin, light polypeptide 7, regulatory
MGI:107495

4 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Hcn2^tm1Ldw/Hcn2^tm2Ldw Myl7^tm1(cre)Krc/Myl7⁺ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal sinoatrial node conduction	J:81398
	irregular heartbeat	J:81398
Mapk14^tm1Lex/Mapk14^tm1Lex Myl7^tm1(cre)Krc/Myl7⁺ involves: 129S1/Sv * 129S5/SvEvBrd * 129X1/SvJ * C57BL/6	abnormal fetal cardiomyocyte proliferation	J:98514
Myl7^tm1(cre)Krc/Myl7⁺ Prkg1^tm2Naw/Prkg1^tm2Naw either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	abnormal cardiac muscle contractility	J:84611

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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