Aliases: DKFZp586E1422.
SLC26A6 (solute carrier family 26 member 6) is named by 1 disorder entry.
The ai-gene-review snapshot this page reads holds 0 core-function terms for SLC26A6; an upstream review of the gene is in progress.
One entry types SLC26A6 as causative: SLC26A6-Related Hyperoxaluria and Nephrolithiasis, and it records the variant as germline. The gene sits on the node Dominant-Negative SLC26A6 Oxalate Transporter Dysfunction, annotated with oxalate transport. ClinGen classifies SLC26A6 for 0 diseases, so no validity tier can be copied onto the record.
Because the function snapshot is empty, the KB node and ai-gene-review share 0 GO terms.
Underlined values are claims re-computed from the knowledge base each time this page is built. The tables below are the source of truth.
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 |
|---|---|---|
| SLC26A6-Related Hyperoxaluria and Nephrolithiasis | causative germline |
mechanism: Dominant-Negative SLC26A6 Oxalate Transporter Dysfunction
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.