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UnknownExpanding the phenotype of TTLL5-associated retinal dystrophy: a case series.
Not available
S-EPMC8973795 | biostudies-literature
UnknownBiallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy.
Not available
S-EPMC4067560 | biostudies-literature
UnknownNovel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy.
Not available
S-EPMC8232641 | biostudies-literature
UnknownNovel pathogenic variants in Tubulin Tyrosine Like 5 (TTLL5) associated with cone-dominant retinal dystrophies and an abnormal optical coherence tomography phenotype.
Not available
S-EPMC10805330 | biostudies-literature
TranscriptomicsDisruption of Ttll5/Stamp gene (Tubulin tyrosine ligase-like protein 5/SRC-1 and TIF2 associated modulatory protein gene) in male mice causes sperm malformation and infertility
Tubulin tyrosine ligase-like family member 5 (TTLL5/STAMP) has multiple activities in cells. TTLL5 is one of 13 TTLLs, has polyglutamylation activity, augments the activity of p160 coactivators (SRC-1 and TIF2) in glucocorticoid receptor-regulated gene induction and repression, and displays steroid-...
ORGANISM(S): Mus musculus 
2013-03-28 | GSE45546 | GEO
UnknownDisruption of Ttll5/stamp gene (tubulin tyrosine ligase-like protein 5/SRC-1 and TIF2-associated modulatory protein gene) in male mice causes sperm malformation and infertility.
Not available
S-EPMC3663537 | biostudies-literature
TranscriptomicsDisruption of Ttll5/Stamp gene (Tubulin tyrosine ligase-like protein 5/SRC-1 and TIF2 associated modulatory protein gene) in male mice causes sperm malformation and infertility
Tubulin tyrosine ligase-like family member 5 (TTLL5/STAMP) has multiple activities in cells. TTLL5 is one of 13 TTLLs, has polyglutamylation activity, augments the activity of p160 coactivators (SRC-1 and TIF2) in glucocorticoid receptor-regulated gene induction and repression, and displays steroid-...
ORGANISM(S): Mus musculus 
2013-03-28 | E-GEOD-45546 | biostudies-arrayexpress
UnknownNovel splice-site mutation in TTLL5 causes cone dystrophy in a consanguineous family.
Not available
S-EPMC5360453 | biostudies-literature
ProteomicsSILAC IP-Mass spectrometry of TTLL-transfected HEK cells
Identification of the non-tubulin substrates of tubulin glycylases, TTLL3/TTLL8 and tubulin glutamylases TTLL4/TTLL5 using SILAC-IP-MS/MS quantitative mass spectrometry approach. HEK cells transfected with the respective enzymes were lysed and the proteins modified by the enzymes enriched by immunop...
ORGANISM(S): Homo sapiens (Human) 
2026-05-18 | PXD065251 | Pride
Hek cells Ttlls Ip-ms/ms Silac 
ProteomicsDifferential modifications of the C-terminal tails of alpha-tubulin isoforms and their importance for kinesin-based microtubule transport in vivo
Microtubules (MTs) are built from alpha/beta-tubulin dimers and used as tracks by kinesin and dynein motors to transport a variety of cargos, such as mRNAs, proteins, and organelles, within the cell. Tubulins are subjected to several post-translational modifications (PTMs). Glutamylation is one of t...
ORGANISM(S): Drosophila melanogaster (Fruit fly) 
2023-07-11 | PXD035270 | Pride
Alpha-tubulin glutamylation In vivo function Axonal transport Ttll5 Microtubule transport Oogenesis 
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