TM4SF19

Gene

transmembrane 4 L six family member 19

HGNCHGNC:25167 EnsemblENSG00000145107 NCBI Gene116211

Locus: gene with protein productLocation: 3q29

Also known as

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

No previous or alternative symbols recorded for this gene.

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.

Retinitis Pigmentosa

Fuchs' Endothelial Dystrophy

Congenital glaucoma

Early-onset non-syndromic cataract

Squamous Cell Carcinoma of Head and Neck

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.

Transmembrane 4 L six family

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.