ZFIN ID: ZDB-FIG-210218-121
Balogh et al., 2020 - Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. Proceedings of the National Academy of Sciences of the United States of America   117(26):15137-15147 Full text @ Proc. Natl. Acad. Sci. USA
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Condition:
Observed In:
Stage Range: Long-pec to Protruding-mouth

Fig. S6 ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

Gene Expression Details No data available
Antibody Labeling Details No data available
Phenotype Details
Fish Conditions Stage Phenotype
TU chemical treatment by environment: cycloheximide Protruding-mouth eye decreased size, abnormal
Protruding-mouth head decreased size, abnormal
Protruding-mouth heart edematous, abnormal
Protruding-mouth optic tectum morphology, abnormal
dkc1elu1/elu1(TU) standard conditions Long-pec whole organism apoptotic process process quality, normal
dkc1elu3/elu3(TU) standard conditions Protruding-mouth eye decreased size, abnormal
Protruding-mouth fourth ventricle swollen, abnormal
Protruding-mouth head decreased size, abnormal
Protruding-mouth heart edematous, abnormal
Acknowledgments:
ZFIN wishes to thank the journal Proceedings of the National Academy of Sciences of the United States of America for permission to reproduce figures from this article. Please note that this material may be protected by copyright. Full text @ Proc. Natl. Acad. Sci. USA