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Publication: Huybrechts et al., 2025 - Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone
All Figures: Figures for Huybrechts et al., 2025

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Figure Caption

Fig. 2 Physical characteristics of sqstm1tmΔUBA zebrafish. a Loss of pigmentation on the flanks and profound redness is evident on the lateral view of sqstm1tmΔUBA/tmΔUBA zebrafish at 6 mpf. This discoloration extends from the snout to the operculum and the chest area. The ventral view shows involvement of the pectoral portion of the ventral side (arrow). b, c Standard length and relative weight of zebrafish at 6 and 12 mpf. Statistical testing was performed using Kruskal–Wallis Tests/Mann–Whitney U Tests. Abbreviations: WT, wild type (sqstm1+/+); HET, heterozygous mutant (sqstm1tmΔUBA/+); HOM, homozygous mutant (sqstm1.tmΔUBA/tmΔUBA)

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Acknowledgments

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