P4HA2

Gene

prolyl 4-hydroxylase subunit alpha 2

HGNCHGNC:8547 EnsemblENSG00000072682 NCBI Gene8974

Locus: gene with protein productLocation: 5q31.1

Also known as

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

Also known aslncRNA-PE · C-P4Halpha(II)

View full nomenclature history (7)

Alias symbolslncRNA-PE, C-P4Halpha(II)

Previous namesprolyl 4-hydroxylase, alpha polypeptide II, procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide II

Alias names4-PH alpha 2, collagen prolyl 4-hydroxylase alpha(II), lncRNA promotes epithelial-mesenchymal transition

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.

Myopia

Dengue

Inflammatory Bowel Diseases

Dermatitis, Atopic

Asthma

Chronic rhinosinusitis

B-cell acute lymphoblastic leukemia

Gout

Rhinitis, Allergic

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.

Iron (II) and 2-oxoglutarate dependent oxygenasesMicroRNA protein coding host genesProlyl 4-hydroxylase subunits

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.