MYO5A
myosin VA
- Ensembl:
- ENSG00000197535
- UniProt:
- Q9Y4I1
- OMIM:
- 160777
- Synonyms:
- GS1, MYH12, MYO5, MYR12
Cilia effects upon perturbation of MYO5A
- Cilia number / % ciliated:
- Decreased cilia number
- Loss-of-function effect:
- Shorter cilia
Ciliogenesis screen results (3 screens)
- Wheway et al. 2015 (siRNA) [siRNA]: Ciliogenesis Defect (z=-3.39) 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:
- abnormal behavior, abnormal cornea morphology, abnormal coat/hair pigmentation
Subcellular localization
basal body, cilia, cytosol, transition zone
Functional category
- Ciliary assembly/disassembly
- Trafficking (BBSome, small GTPases, vesicular transport, ATPases)
- Actin & cytoskeleton regulation
- Metabolism
- Viral interactions
- Signaling (Hedgehog, GPCRs, ion channels)
- Transition zone
- Transcription regulation
Function
Knockout results in reduction in ciliation, suggesting MYO5A is required for ciliogenesis. It might link microtubule cargo from Golgi or cilium (28710093). It mediates the transportation of preciliary vesicles to the mother centriole, depletion inhibits the attachment of preciliary vesicles to the distal appendages of the mother centriole and decreases cilia assembly (29335527). Interacts with the cilia- centrosomal protein RPGRIP1L (28266547).