Kcnv2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kcnv2
potassium channel, subfamily V, member 2
MGI:2670981

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnv2^{tm1.1(KOMP)Wtsi}/Kcnv2^{tm1.1(KOMP)Wtsi} involves: C57BL/6NTac	no abnormal phenotype detected	J:82809
Kcnv2^{tm1.2(KOMP)Wtsi}/Kcnv2^{tm1.2(KOMP)Wtsi} involves: 129S6/SvEvTac * C57BL/6N	abnormal cone electrophysiology	J:279816
	abnormal rod electrophysiology	J:279816
	decreased retina rod cell number	J:279816
	decreased total retina thickness	J:279816
	increased retina apoptosis	J:279816
	short photoreceptor inner segment	J:279816
	short photoreceptor outer segment	J:279816
	thin retina outer nuclear layer	J:279816

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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