MPDU1

Gene

mannose-P-dolichol utilization defect 1

HGNCHGNC:7207 EnsemblENSG00000129255 NCBI Gene9526

Locus: gene with protein productLocation: 17p13.1

Also known as

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

Also known asSL15 · Lec35 · PQLC5 · CDGIf · SLC66A5

View full nomenclature history (5)

Alias symbolsSL15, Lec35, PQLC5, CDGIf, SLC66A5

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.

Congenital disorder of glycosylation

SRD5A3-congenital disorder of glycosylation

Genetic Diseases, Inborn

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.

Solute carrier family 66

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-14.

Open TargetsGene–disease associations from the Open Targets Platform.