| Category | Gene | Protein/Syndrome Disease | Inheritance | OMIM # |
|---|---|---|---|---|
| HPABH4D/RCAD-like | PCBD1 | PCBD1 | AR | 126090 |
| ADTKD/RCAD | HNF1B | HNF1β | AD | 189907 |
| Isolated dominant hypomagnesemia | FXYD2 | γ-subunit of the Na/K-ATPase | AD | 601814 |
| EAST syndrome | KCNJ10 | Kir4.1 | AR | 602208 |
| Bartter syndrome, type 4 | BSND | Barttin | AR | 606412 |
| Gitelman syndrome | SLC12A3 | NCC | AR | 600968 |
