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TCTN3

Gene

tectonic family member 3

HGNCHGNC:24519EnsemblENSG00000119977NCBI Gene26123
Locus: gene with protein productLocation: 10q24.1

Also known as

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

Also known asC10orf61 · DKFZP564D116 · TECT3 · JBTS18
View full nomenclature history (5)
Previous symbolsC10orf61
Alias symbolsDKFZP564D116, TECT3, JBTS18
Previous nameschromosome 10 open reading frame 61

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.

Ciliopathy
Genetic Diseases, Inborn

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.

Tectonic 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.