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CSTPP1

Gene

centriolar satellite-associated tubulin polyglutamylase complex regulator 1

HGNCHGNC:28720EnsemblENSG00000149179NCBI Gene79096
Locus: gene with protein productLocation: 11p11.2

Also known as

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

Also known asC11orf49 · FLJ22210 · MGC4707
View full nomenclature history (5)
Previous symbolsC11orf49
Alias symbolsFLJ22210, MGC4707
Previous nameschromosome 11 open reading frame 49
Alias namescentriolar satellite-associated tubulin polyglutamylation protein 1

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.

Thrombophilia
Venous Thrombosis
Venous Thromboembolism
Hypertension
Colitis, Ulcerative
Inflammatory Bowel Diseases
Kidney Failure, Chronic
Cardiomyopathies

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.

Centriolar satellite proteins

Provenance

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