KIF6

kinesin family member 6

Ensembl:
ENSG00000164627
UniProt:
Q6ZMV9
OMIM:
613919
Synonyms:
C6ORF102, DJ1043E3.1, DJ137F1.4, DJ188D3.1, DKFZP451I2418

Cilia effects upon perturbation of KIF6

Cilia number / % ciliated:
Unknown
Loss-of-function effect:
Unknown
Overexpression effect:
Unknown

Ciliogenesis screen results (2 screens)

  • Wheway et al. 2015 (siRNA) [siRNA]: No effect PMID:26167766
  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680

Phenotypes

Mouse phenotype:
small heart, decreased brain size
Mouse ciliopathy phenotype:
abnormal uterus morphology, abnormal brain morphology, female infertility, small testis, male infertility, abnormal testis morphology, hydrocephaly, hydrometra, abnormal heart morphology

Subcellular localization

cilia, nucleus

Functional category

  • Ciliary assembly/disassembly
  • Actin & cytoskeleton regulation
  • Metabolism

Function

Mediator of ciliogenesis and normal cilia beating in ependmal cells in vertebrates. Mutations are reported to be associated with neurological abnormalities in humans (30475797).

Model organism evidence

Mus musculus (2 references)

Here, we show that Kif6 is a slow processive motor (12.2±2.0 nm/s) on microtubules in vitro and localizes to both the apical cytoplasm and the axoneme in ependymal cells, although it does not display processive movement in vivo.

We find that loss of Kif6 function caused decreased ependymal cilia motility and subsequently decreased fluid flow on the surface of brain ventricular walls.

PMIDs: 38235522, 36824804