Kcnj13 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kcnj13
potassium inwardly-rectifying channel, subfamily J, member 13
MGI:3781032

17 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnj13^{tm1(KOMP)Vlcg}/Kcnj13^{tm1(KOMP)Vlcg} involves: C57BL/6NTac	abnormal lung saccule morphology	J:227219
	abnormal palatal shelf fusion at midline	J:227219
	absent maxillary shelf	J:227219
	absent palatine bone horizontal plate	J:227219
	absent suckling reflex	J:227219
	cleft secondary palate	J:227219
	decreased birth body size	J:227219
	decreased fetal size	J:227219
	neonatal lethality, complete penetrance	J:227219
	palatal shelves fail to meet at midline	J:227219
	normal respiratory system phenotype	J:227219
	small lung saccule	J:227219
Kcnj13^{tm1b(KOMP)Wtsi}/Kcnj13^{tm1b(KOMP)Wtsi} C57BL/6N-Kcnj13^{tm1b(KOMP)Wtsi}/Bay	abnormal embryo size	J:211773
	abnormal head shape	J:211773
	cleft palate	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete penetrance	J:211773

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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