ZFIN ID: ZDB-FIG-210325-50
Xia et al., 2019 - Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway. FEBS letters   593(15):2008-2018 Full text @ FEBS Lett.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage: Long-pec

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
s356tTg + MO2-top2b standard conditions Long-pec neuromast decreased amount, abnormal
Long-pec neuromast hair cell decreased amount, abnormal
Long-pec neuromast support cell decreased amount, abnormal
s356tTg + MO3-top2b standard conditions Long-pec neuromast decreased amount, abnormal
Long-pec neuromast hair cell decreased amount, abnormal
Long-pec neuromast support cell decreased amount, abnormal
Full text @ FEBS Lett.