Kcnj2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Kcnj2
potassium inwardly-rectifying channel, subfamily J, member 2
MGI:104744

14 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnj2^tm1Swz/Kcnj2⁺ involves: 129S1/Sv * 129X1/SvJ * FVB	abnormal intramembranous bone ossification	J:314753
Kcnj2^tm1Swz/Kcnj2⁺ involves: 129S1/Sv * 129X1/SvJ * FVB	decreased maxillary shelf size	J:314753
Kcnj2^tm1Swz/Kcnj2^tm1Swz involves: 129S1/Sv * 129X1/SvJ * FVB	abnormal digit morphology	J:314753
	abnormal suckling behavior	J:78077
	abnormal vasodilation	J:78077
	cleft secondary palate	J:78077, J:314753
	cyanosis	J:78077
	decreased maxillary shelf size	J:314753
	dehydration	J:78077
	narrow maxilla	J:78077
	neonatal lethality, complete penetrance	J:78077
	palatal shelves fail to meet at midline	J:78077
	preaxial polydactyly	J:314753
	respiratory distress	J:78077
	small vomer bone	J:314753

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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