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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 | Hypomagnesemia |
Hypokalemia |
Hypochloremia |
Increased serum prostaglandin E2 |
Hypokalemic metabolic alkalosis |
Dehydration |
Fever |
Hyperchloriduria |
Increased urinary potassium |
Renal potassium wasting |
Hypercalciuria |
Renal salt wasting |
Hyperprostaglandinuria |
Hyposthenuria |
Chondrocalcinosis |
| Disease(s) Associated with KCNJ1 | |||||||||||||||
| Bartter disease type 2 |
| Mouse Phenotypes | increased circulating sodium level |
dehydration |
metabolic acidosis |
abnormal urine homeostasis |
decreased urine osmolality |
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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 09/03/2024 MGI 6.24 |
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