ZFIN ID: ZDB-FIG-210212-2
Xia et al., 2019 - Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss. Clinical genetics   96(4):300-308 Full text @ Clin. Genet.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagent:
Observed In:
Stage Range: Long-pec to Day 5

Fig. 3 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 + MO2-trrap standard conditions Long-pec neuromast decreased amount, abnormal
Long-pec neuromast decreased size, abnormal
Long-pec neuromast support cell amount, normal
Long-pec somite morphology, normal
Day 5 neuromast hair cell kinocilium decreased amount, abnormal
Day 5 neuromast hair cell kinocilium decreased length, abnormal
Day 5 neuromast hair cell stereocilium decreased amount, abnormal
Day 5 neuromast hair cell stereocilium decreased length, abnormal
Day 5 neuromast hair cell stereocilium decreased thickness, abnormal
trrapzf3166/+ standard conditions Long-pec neuromast decreased amount, abnormal
Long-pec neuromast decreased size, abnormal
Long-pec neuromast hair cell kinocilium decreased amount, abnormal
Long-pec neuromast hair cell kinocilium decreased length, abnormal
Long-pec somite morphology, normal
Day 5 neuromast hair cell stereocilium decreased amount, abnormal
Day 5 neuromast hair cell stereocilium decreased length, abnormal
Day 5 neuromast hair cell stereocilium decreased thickness, abnormal
trrapzf3166/+; s356tTg standard conditions Long-pec neuromast hair cell decreased amount, abnormal
Long-pec neuromast support cell decreased amount, abnormal
Full text @ Clin. Genet.