Back to discover

ATP10D

Gene

ATPase phospholipid transporting 10D (putative)

HGNCHGNC:13549EnsemblENSG00000145246NCBI Gene57205
Locus: gene with protein productLocation: 4p12

Also known as

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

Also known asATPVD · KIAA1487
View full nomenclature history (4)
Alias symbolsATPVD, KIAA1487
Previous namesATPase, Class V, type 10D
Alias namesphospholipid-transporting ATPase VD

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.

Pre-Eclampsia
Parkinson's Disease
Parasitic Diseases
Lysosomal Storage Diseases
Neurodegenerative Diseases
Alzheimer's Disease
Multiple Sclerosis
Vascular Diseases

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.

ATPase phospholipid transporting

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-11-19.
Open TargetsGene–disease associations from the Open Targets Platform.