TEN1

Gene

TEN1 subunit of CST complex

HGNCHGNC:37242 EnsemblENSG00000257949 NCBI Gene100134934

Locus: gene with protein productLocation: 17q25.1

Also known as

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

Also known asC17orf106 · FLJ39785

View full nomenclature history (6)

Previous symbolsC17orf106

Alias symbolsFLJ39785

Previous namesTEN1 telomerase capping complex subunit homolog (S. cerevisiae), chromosome 17 open reading frame 106, TEN1 CST complex subunit, TEN1, CST complex subunit

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.

Neurodegenerative Diseases

Hypothyroidism

Neoplasms

Dyskeratosis congenita

Cockayne Syndrome

Genetic developmental and epileptic encephalopathy

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.

CST complex

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.