FIGURE
Fig. S11
- ID
- ZDB-FIG-180516-28
- Publication
- Ojeda Naharros et al., 2017 - Loss-of-function of the ciliopathy protein Cc2d2a disorganizes the vesicle fusion machinery at the periciliary membrane and indirectly affects Rab8-trafficking in zebrafish photoreceptors
- Other Figures
- All Figure Page
- Back to All Figure Page
Fig. S11
Comparison of cc2d2a and ift88 mutant retinae indicates that vesicle accumulation in PRs is not a general non-specific defect secondary to any ciliary dysfunction. (A-C) Transmission electron microscopy images of 3 dpf wild-type (A), cc2d2a mutant (B) and ift88 mutant (C) retinae. Note the accumulation of vesicular structures and abnormal membrane stacks in cc2d2a mutants, while no vesicles are found in the inner segments of ift88 mutants. |
Expression Data
Expression Detail
Antibody Labeling
Phenotype Data
Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and
ZFIN has permission only to display this image to its users.
Additional permissions should be obtained from the applicable author or publisher of the image.
Full text @ PLoS Genet.