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.
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
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.