SLC4A11

Gene

solute carrier family 4 member 11

HGNCHGNC:16438 EnsemblENSG00000088836 NCBI Gene83959

Locus: gene with protein productLocation: 20p13

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asCHED2 · CDPD1 · dJ794I6.2 · BTR1 · NaBC1 · FECD4

View full nomenclature history (12)

Previous symbolsCHED2, CDPD1

Alias symbolsdJ794I6.2, BTR1, NaBC1, FECD4

Previous namescorneal endothelial dystrophy 2 (autosomal recessive), solute carrier family 4, sodium bicarbonate transporter-like, member 11, corneal dystrophy and perceptive deafness 1, solute carrier family 4, sodium borate transporter, member 11

Alias namesbicarbonate transporter related protein 1, sodium-coupled borate cotransporter 1

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Fuchs' Endothelial Dystrophy

Corneal Dystrophies, Hereditary

Genetic Diseases, Inborn

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 4

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.