SIX1

SIX homeobox 1

Ensembl:
ENSG00000126778
UniProt:
Q15475
OMIM:
601205
Synonyms:
DFNA23

Cilia effects upon perturbation of SIX1

Ciliogenesis screen results (5 screens)

  • Kim2016: Not Reported
  • Wheway et al. 2015 (siRNA) [siRNA]: No effect PMID:26167766
  • Breslow et al. 2018 (CRISPR) [CRISPR]: No Significant Effect PMID:29459680
  • Roosing et al. 2015 (siRNA) [siRNA]: No effect PMID:26595381
  • Kim et al. 2010 (siRNA) [siRNA]: Shorter Cilia (Area per Cilia z=-2.73) PMID:20393562

Phenotypes

Human ciliopathy phenotype:
autosomal dominant nonsyndromic hearing loss

Subcellular localization

cilia, nucleoli, nucleoplasm

Function

SIX1 has located to motile cilia.