ZFIN ID: ZDB-FIG-160617-1
Wu et al., 2016 - Haploinsufficiency of RCBTB1 is Associated with Coats Disease and Familial Exudative Vitreoretinopathy. Human Molecular Genetics   25(8):1637-47 Full text @ Hum. Mol. Gen.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage Range: Protruding-mouth to Day 4

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 DetailsNo data available
Antibody Labeling Details No data available
Phenotype Details
Fish Conditions Stage Phenotype
y1Tg + MO1-ndp standard conditions Day 4 ocular blood vessel decreased area, abnormal
Day 4 ocular blood vessel morphology, abnormal
y1Tg + MO1-ndp + MO1-rcbtb1 standard conditions Day 4 ocular blood vessel decreased area, abnormal
Day 4 ocular blood vessel morphology, abnormal
y1Tg + MO1-rcbtb1 standard conditions Protruding-mouth intersegmental vessel decreased thickness, abnormal
Protruding-mouth intersegmental vessel morphology, abnormal
Protruding-mouth intersegmental vessel truncated, abnormal
Day 4 intersegmental vessel decreased thickness, abnormal
Day 4 intersegmental vessel morphology, abnormal
Day 4 ocular blood vessel decreased area, abnormal
Day 4 ocular blood vessel morphology, abnormal
Full text @ Hum. Mol. Gen.