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HNRNPH2

Gene

heterogeneous nuclear ribonucleoprotein H2

HGNCHGNC:5042EnsemblENSG00000126945NCBI Gene3188
Locus: gene with protein productLocation: Xq22.1

Also known as

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

Also known asHNRPH2 · hnRNPH' · FTP3 · HNRPH'
View full nomenclature history (5)
Previous symbolsHNRPH2
Alias symbolshnRNPH', FTP3, HNRPH'
Previous namesheterogeneous nuclear ribonucleoprotein H2 (H')

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.

Neurodevelopmental Disorders
Genetic Diseases, Inborn
Dengue
Fabry Disease

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.

RNA binding motif containingHeterogeneous nuclear ribonucleoproteins

Provenance

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