PYROXD1

Gene

pyridine nucleotide-disulphide oxidoreductase domain 1

HGNCHGNC:26162 EnsemblENSG00000121350 NCBI Gene79912

Locus: gene with protein productLocation: 12p12.1

Also known as

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

Also known asDKFZp762G094 · FLJ22028

View full nomenclature history (2)

Alias symbolsDKFZp762G094, FLJ22028

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.

Muscular dystrophy

Inherited cancer-predisposing syndrome

Neoplastic Syndromes, Hereditary

Genetic Diseases, Inborn

Neurodegenerative 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.

Flavoproteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.