Kcnk13 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kcnk13
potassium channel, subfamily K, member 13
MGI:2384976

6 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnk13^em1(IMPC)H/Kcnk13^em1(IMPC)H C57BL/6N-Kcnk13^em1(IMPC)H/H	increased basophil cell number	J:211773
	increased mean corpuscular volume	J:211773
	increased monocyte cell number	J:211773
	increased red blood cell distribution width	J:211773
Kcnk13^em1(IMPC)H/Kcnk13^em1(IMPC)H involves: C57BL/6NTac	abnormal microglial cell morphology	J:256020
Kcnk13^em1(IMPC)H/Kcnk13^em1(IMPC)H involves: C57BL/6NTac	abnormal microglial cell physiology	J:256020

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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