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SNX27

Gene

sorting nexin 27

HGNCHGNC:20073EnsemblENSG00000143376NCBI Gene81609
Locus: gene with protein productLocation: 1q21.3

Also known as

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

Also known asMY014 · KIAA0488 · MGC20471
View full nomenclature history (4)
Alias symbolsMY014, KIAA0488, MGC20471
Previous namessorting nexin family member 27

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.

Epilepsies, Myoclonic
Dermatitis, Atopic
Genetic Diseases, Inborn
Carcinoma, Hepatocellular
Down Syndrome

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 nexinsPDZ domain containing

Provenance

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