KCNJ1
| Deellabo: | PGD DNA |
| Gen (Gen Code): | KCNJ1 |
| Aliases Gen: | KIR1.1, ROMK, ROMK1 |
| Gen ID (NCBI): | 3758 |
| OMIM Gen ID: | 600359 |
| Chromosomale locatie: | 11q24 |
| Genetische aandoening / Analyse: | Bartter syndroom type 2 |
| OMIM aandoening ID: | 241200 |
| Overerving: | AR |
| Aliases aandoening: | BARTTER SYNDROME, ANTENATAL, TYPE 2 HYPOKALEMIC ALKALOSIS WITH HYPERCALCIURIA, ANTENATAL, 2 HYPERPROSTAGLANDIN E SYNDROME 2 |