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TTLL5

Gene

tubulin tyrosine ligase like 5

HGNCHGNC:19963EnsemblENSG00000119685NCBI Gene23093
Locus: gene with protein productLocation: 14q24.3

Also known as

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

Also known asSTAMP
View full nomenclature history (5)
Alias symbolsSTAMP
Previous namesKIAA0998, tubulin tyrosine ligase-like family member 5
Alias namestubulin polyglutamylase TTLL5, SRC1 and TIF2-associated modulatory protein

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.

Cone rod dystrophy
Cone-rod dystrophy
Retinitis Pigmentosa
Carpal Tunnel Syndrome
Placental abruption

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.

Tubulin tyrosine ligase family

Provenance

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