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Symbol
Name
ID
Kcnj1
potassium inwardly-rectifying channel, subfamily J, member 1
MGI:1927248
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Polydipsia
Disease(s) Associated with KCNJ1
Bartter disease type 2

Mouse Phenotypes
polydipsia
Availability Mouse Genotype
Kcnj1tm1Ges/Kcnj1tm1Ges

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory