ZFIN ID: ZDB-FIG-120412-48
Coon et al., 2012 - The Lowe Syndrome Protein OCRL1 is Involved in Primary Cilia Assembly. Human molecular genetics   21(8):1835-1847 Full text @ Hum. Mol. Genet.
ADDITIONAL FIGURES
PHENOTYPE:
Fish:
Knockdown Reagents:
Observed In:
Stage Range: Prim-5 to Days 7-13

Fig. S1 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/TL + MO2-ocrl standard conditions Long-pec eye decreased size, abnormal
Long-pec head decreased size, abnormal
Long-pec melanocyte decreased amount, abnormal
Long-pec melanocyte mislocalised, abnormal
Long-pec whole organism curled, abnormal
Long-pec whole organism anterior-posterior axis decreased length, abnormal
ba2Tg + MO3-ocrl standard conditions Prim-5 neural crest cell migration disrupted, abnormal
ocrlumc5Tg/umc5Tg standard conditions Days 7-13 neuromast immature, abnormal
Full text @ Hum. Mol. Genet.