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SNX19

Gene

sorting nexin 19

HGNCHGNC:21532EnsemblENSG00000120451NCBI Gene399979
Locus: gene with protein productLocation: 11q24.3-q25

Also known as

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

Also known asKIAA0254 · CHET8
View full nomenclature history (2)
Alias symbolsKIAA0254, CHET8

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.

Schizophrenia
Obesity disorder
Diabetes Mellitus
Autism Spectrum Disorder
Spinal Cord Injuries
Tinea
Obesity, Morbid
Anorexia Nervosa
Diabetes Mellitus, Type 2

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.

Sorting nexins

Provenance

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