Beck et al., 2014 - Mutation of POC1B in a Severe Syndromic Retinal Ciliopathy. Human Mutation   35(10):1153-62 Full text @ Hum. Mutat.

Fig. 5 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.

PHENOTYPE:
Fish: AB/TU + MO1-poc1b, AB/TU + MO2-poc1b
Knockdown Reagents: MO1-poc1b, MO2-poc1b
Observed In: cilium assembly, eye, head, kidney, melanocyte (all 15) expand
Stage Range: Day 4 to Day 5
Full text @ Hum. Mutat.