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PPP1R17

Gene

protein phosphatase 1 regulatory subunit 17

HGNCHGNC:16973EnsemblENSG00000106341NCBI Gene10842
Locus: gene with protein productLocation: 7p14.3

Also known as

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

Also known asC7orf16 · GSBS
View full nomenclature history (5)
Previous symbolsC7orf16
Alias symbolsGSBS
Previous nameschromosome 7 open reading frame 16, protein phosphatase 1, regulatory subunit 17
Alias namesG-substrate

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.

Subarachnoid Hemorrhage
Premature Birth
Lung Diseases
Female reproductive system disorder
Psoriasis
Ovarian neoplasm

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.

Protein phosphatase 1 regulatory 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.