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SLC44A3

Gene

solute carrier family 44 member 3

HGNCHGNC:28689EnsemblENSG00000143036NCBI Gene126969
Locus: gene with protein productLocation: 1p21.3

Also known as

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

Also known asMGC45474 · CTL3
View full nomenclature history (4)
Alias symbolsMGC45474, CTL3
Previous namessolute carrier family, member 3, solute carrier family 44, member 3

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.

Thyroiditis, Autoimmune
Enteritis
Hemorrhoid
Retinitis Pigmentosa
Early-onset non-syndromic cataract
Cone rod dystrophy
Posterior polar cataract

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 44

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.