ZFIN ID: ZDB-FIG-151104-5
Abrams et al., 2015 - Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics   47(8):926-32 Full text @ Nat. Genet.
Knockdown Reagent:
Observed In:
Stage: Long-pec

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.

Gene Expression Details No data available
Antibody Labeling Details No data available
Phenotype Details
Fish Conditions Stage Phenotype
WT + MO1-slc25a46 standard conditions Long-pec motor neuron bleb assembly process quality, abnormal
vu19Tg + MO1-slc25a46 standard conditions Long-pec motor neuron axon decreased length, abnormal
Long-pec spinal cord neuron projection decreased amount, abnormal
zc7Tg + MO1-slc25a46 standard conditions Long-pec retinal ganglion cell axon shortened, abnormal
Full text @ Nat. Genet.