KIF11
kinesin family member 11
Tier: Gold Standard Ciliary Genes
- Ensembl:
- ENSG00000138160
- UniProt:
- P52732
- OMIM:
- 148760
- Synonyms:
- EG5, HKSP, KNSL1, TRIP5
Cilia effects upon perturbation of KIF11
- Cilia number / % ciliated:
- Incrased cilia number
- Loss-of-function effect:
- Longer cilia
Ciliogenesis screen results (4 screens)
- Kim2016: No effect
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-4.92) PMID:26167766
- Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
- Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
Phenotypes
- Human ciliopathy phenotype:
- microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
Subcellular localization
basal body, cilia, cytosol, microtubules, ribosome
References: PMID:41005307, PMID:9701554, PMID:23857769, PMID:32811879
Functional category
- Ciliary assembly/disassembly
- Actin & cytoskeleton regulation
- Axon guidance & growth
Function
KIF11 has been demonstrated to have microtubule polymerase activity, as well as to control axon growth(26437877, 17846176). It has also been shown to mediate centrosome migration after mitosis and move Golgi material(9701554 , 23857769). An interphase pool of KIF11 localizes at the basal bodies of primary cilia and a reduction in KIF11 expression alters cilia dynamics(32811879).Upon the reduction of KIF11 expression, the number of ciliated cells in asynchronously growing populations was significantly increased. Depleting KIF11 resulted in an increase in cilium length and an attenuation in the kinetics of cilia disassembly(PMID: 32811879).