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VPS13D

Gene

vacuolar protein sorting 13 homolog D

HGNCHGNC:23595EnsemblENSG00000048707NCBI Gene55187
Locus: gene with protein productLocation: 1p36.22-p36.21

Also known as

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

Also known asFLJ10619 · KIAA0453 · BLTP5D
View full nomenclature history (6)
Alias symbolsFLJ10619, KIAA0453, BLTP5D
Previous namesvacuolar protein sorting 13D (yeast), vacuolar protein sorting 13 homolog D (S. cerevisiae)
Alias namesbridge-like lipid transfer protein family member 5D

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.

Neurodegenerative Diseases
Genetic Diseases, Inborn
Gastritis, Atrophic
Infertility, Male

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.

Small nucleolar RNA protein coding host genesBridge-like lipid transfer protein family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-01-16.
Open TargetsGene–disease associations from the Open Targets Platform.