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Symbol
Name
ID
Kcnj1
potassium inwardly-rectifying channel, subfamily J, member 1
MGI:1927248
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Hypercalciuria
Hyperchloriduria
Increased urinary potassium
Renal potassium wasting
Renal salt wasting
Hyposthenuria
Renal juxtaglomerular cell hypertrophy/hyperplasia
Nephrocalcinosis
Polyuria
Disease(s) Associated with KCNJ1
Bartter disease type 2

Mouse Phenotypes
abnormal urine homeostasis
decreased urine osmolality
hydronephrosis
decreased renal glomerular filtration rate
decreased tubuloglomerular feedback response
polyuria
Availability Mouse Genotype
Kcnj1tm1Ges/Kcnj1tm1Ges

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory