FIGURE

Fig. S2

ID

ZDB-FIG-100504-33

Publication

Carney et al., 2010 - Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel Fraser Syndrome disease genes

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Fig. S2

Pectoral and adult tail fin phenotypes. (A–I) Lateral views of pectoral fins at 72 hpf showing the blisters (red arrows) present in pif^te262/te262 (B), pif^tm95/ttm95 (C), bla^ta90/ta90 (D), nel^tq207/tq207 (E), stu^td204/td204 (F) and rfl^fr23/fr23 (G) embryos compared to WT (A). The dysmorphogenesis of the pectoral pins in fra^tc17/tc17 (H) and bdf^fr21/fr21 (I) is highlighted with the edge of the fin circumscribed by red dashed line, clearly showing the reduction of the fin compared to WT (A). (J–O) Adult fin phenotypes at 96 dpf: the tail fins of pif^tm95/ttm95 (K) and bdf^fr21/fr21 (O) mutants are reduced compared to WT (J), bla^ta90/ta90 (L), nel^tq207/tq207 (M) and rfl^fr23/fr23 (N).

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Phenotype Detail

Acknowledgments

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