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. 2021 Nov 11;220(12):e202104087. doi: 10.1083/jcb.202104087

Table 2. Analyses of patterning defects in retinas.

Genotype Patterning errors per data point Total errors per data point (ommatidium + surrounding lattice)
Cone cell defects (1) 1° cell defects (2) Ommatidial misorientations (3) Bristle defects (4) 3° cell defects (5) Errors in lattice cell number (6)
Mean SD Mean SD Mean SD Mean SD Mean SD Mean SD Mean SD SE Comparison with cnoWT-GFP (P value)
w1118 0.00 0.00 0.02 0.18 0.00 0.00 0.28 0.45 0.10 0.30 0.21 0.46 0.61 0.94 0.09 0.8087
w1118; cnoWT-GFP 0.01 0.09 0.01 0.09 0.00 0.00 0.27 0.48 0.07 0.25 0.22 0.45 0.58 0.94 0.09
w1118; cno△PDZ-GFP 0.30 0.62 0.21 0.52 0.08 0.27 0.69 0.72 0.68 0.78 0.65 0.77 2.61 2.40 0.22 <0.0001
w1118; cno△FAB-GFP 0.13 0.40 0.16 0.61 0.02 0.13 0.34 0.56 0.16 0.43 0.23 0.91 1.03 1.68 0.15 0.0106

The following defects were scored in 118 data points (illustrated in Fig. 9) per genotype: (1) errors in cone cell number and arrangement; (2) incorrect number, relative size and junctional integrity of 1° cells; (3) incorrect orientation of ommatidial core (likely due to earlier mis-rotation); (4) errors in bristle placement and number; (5) incorrect specification of 3° cells; (6) additional or missing lattice cells (2° cells + 3° cells).