Aliases: hClC-Kb, CLCKB, ClC-K2, ClC-Kb.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Bartter syndrome | causative |
mechanism: ClC-K/Barttin Chloride Channel Dysfunction (Type 4); ClC-Kb Basolateral Chloride Exit Failure (Type 3)
subtype: Type 3; Type 4B
scoped to subtype: Type 3
|
| Gitelman syndrome |
untyped
Gitelman-like loss-of-function variant
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.