KCTD17
potassium channel tetramerization domain containing 17
- Ensembl:
- ENSG00000100379
- UniProt:
- Q8N5Z5
- OMIM:
- 616386
- Synonyms:
- FLJ12242
Cilia effects upon perturbation of KCTD17
- Loss-of-function effect:
- Shorter cilia
Ciliogenesis screen results (4 screens)
- Kim2016: Not Reported
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-3.56) PMID:26167766
- Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
- Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
Phenotypes
- Mouse phenotype:
- absent vibrissae
Subcellular localization
basal body
Functional category
- Ciliary assembly/disassembly
Function
Substrate-adaptor for Cul3- RING E3 ligases (CRL3s) that modulates polyubiquitylation of trichoplein and e bles cells to assemble primary cilia by limiting Aurora-A activity. KCTD17 is required to initiate the axoneme extension during ciliogenesi (25270598). Depletion of KCTD17 specifically arrests ciliogenesis at the initial step of axoneme extension through aberrant trichoplein–Aurora-A activity. Knockdown of KCTD17 shortened primary cilia of hTERT-RPE1 cells through inhibition of proteolysis of TCHP. (37780208)