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Symbol Name ID |
Kcnj1
potassium inwardly-rectifying channel, subfamily J, member 1 MGI:1927248 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hyperchloriduria |
Increased urinary potassium |
Renal potassium wasting |
Hypercalciuria |
Renal salt wasting |
Hyperprostaglandinuria |
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 |
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| Availability | Mouse Genotype | ||||||
| Kcnj1tm1Ges/Kcnj1tm1Ges | |||||||
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 08/02/2024 MGI 6.24 |
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