Kcnh2 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kcnh2
potassium voltage-gated channel, subfamily H (eag-related), member 2
MGI:1341722

17 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnh2^tm1.1Hjd/Kcnh2^tm1.1Hjd involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal aortic sac morphology	J:155273
	abnormal blood circulation	J:155273
	abnormal bulbus cordis morphology	J:155273
	abnormal cardiac outflow tract development	J:155273
	abnormal cardiovascular system physiology	J:155273
	abnormal craniofacial morphology	J:155273
	abnormal first pharyngeal arch morphology	J:155273
	abnormal heart development	J:155273
	abnormal heart looping	J:155273
	abnormal heart morphology	J:155273
	abnormal muscle electrophysiology	J:155273
	decreased embryo size	J:155273
	dilated aortic sac	J:155273
	embryonic lethality during organogenesis, complete penetrance	J:155273
	irregular heartbeat	J:155273
	pericardial effusion	J:155273
	small first pharyngeal arch	J:155273

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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