ZFIN ID: ZDB-FIG-170602-31
Ma et al., 2017 - SLC44A4 Mutation Causes Autosomal Dominant Hereditary Postlingual Non-syndromic Mid-frequency Hearing loss. Human molecular genetics   26(2):383-394 Full text @ Hum. Mol. Genet.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage Range: Protruding-mouth to Day 5

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
AB + MO1-slc44a4 standard conditions Protruding-mouth inner ear decreased size, abnormal
Protruding-mouth otolith decreased size, abnormal
Protruding-mouth otolith fused with otolith, abnormal
Protruding-mouth otolith mislocalised, abnormal
Day 5 startle response process quality, abnormal
Day 5 swimming behavior process quality, abnormal
AB + MO2-slc44a4 standard conditions Protruding-mouth inner ear decreased size, abnormal
Protruding-mouth otolith decreased size, abnormal
Protruding-mouth otolith fused with otolith, abnormal
Protruding-mouth otolith mislocalised, abnormal
Day 5 startle response process quality, abnormal
Day 5 swimming behavior process quality, abnormal
s356tTg + MO1-slc44a4 standard conditions Day 5 neuromast decreased amount, abnormal
Day 5 neuromast decreased size, abnormal
Day 5 neuromast hair cell decreased amount, abnormal
Day 5 neuromast hair cell stereocilium decreased amount, abnormal
Day 5 somite development process quality, normal
s356tTg + MO2-slc44a4 standard conditions Day 5 neuromast decreased amount, abnormal
Day 5 neuromast decreased size, abnormal
Day 5 neuromast hair cell decreased amount, abnormal
Day 5 neuromast hair cell stereocilium decreased amount, abnormal
Day 5 somite development process quality, normal
Full text @ Hum. Mol. Genet.