ZFIN ID: ZDB-FIG-180404-41
Louw et al., 2018 - Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings. PLoS Genetics   14:e1007138 Full text @ PLoS Genet.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage Range: Long-pec to Day 6

Unillustrated author statements

Gene Expression Details No data available
Antibody Labeling Details No data available
Phenotype Details
Fish Conditions Stage Phenotype
WT + MO1-kif20a standard conditions Long-pec brain edematous, abnormal
Long-pec trunk decreased length, abnormal
Long-pec whole organism decreased length, abnormal
Day 6 heart decreased functionality, abnormal
Day 6 pericardium edematous, abnormal
WT + MO1-kif20a + MO4-tp53 standard conditions Day 4 heart decreased functionality, abnormal
Day 4 pericardium edematous, abnormal
Acknowledgments:
ZFIN wishes to thank the journal PLoS Genetics for permission to reproduce figures from this article. Please note that this material may be protected by copyright. Full text @ PLoS Genet.