ZFIN ID: ZDB-FIG-180710-44
Brockmann et al., 2018 - CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency. Human molecular genetics   27(4):706-715 Full text @ Hum. Mol. Genet.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage: Protruding-mouth

Fig. 4 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
WT + MO1-chchd10 standard conditions Protruding-mouth skeletal muscle mitochondrion morphology, normal
Protruding-mouth skeletal muscle refractivity, abnormal
Protruding-mouth skeletal muscle skeletal muscle myofibril disorganized, abnormal
Protruding-mouth thigmotaxis disrupted, abnormal
WT + MO2-chchd10 standard conditions Protruding-mouth skeletal muscle mitochondrion morphology, normal
Protruding-mouth skeletal muscle refractivity, abnormal
Protruding-mouth skeletal muscle skeletal muscle myofibril disorganized, abnormal
Protruding-mouth thigmotaxis disrupted, abnormal
Full text @ Hum. Mol. Genet.