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P3H2

Gene

prolyl 3-hydroxylase 2

HGNCHGNC:19317EnsemblENSG00000090530NCBI Gene55214
Locus: gene with protein productLocation: 3q28

Also known as

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

Also known asLEPREL1 · FLJ10718 · MLAT4
View full nomenclature history (5)
Previous symbolsLEPREL1
Alias symbolsFLJ10718, MLAT4
Previous namesleprecan-like 1
Alias namesprocollagen-proline 3-dioxygenase 2

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.

Osteoarthritis, Hip
Retinitis Pigmentosa
Osteoarthritis, Knee
Total joint arthroplasty
Placental retention

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 oxygenasesProlyl 3-hydroxylase family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.