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. Author manuscript; available in PMC: 2017 Aug 1.
Published in final edited form as: Dev Biol. 2016 Jun 2;416(1):136–148. doi: 10.1016/j.ydbio.2016.05.035

Table 1.

itga8 mutant fish show partially penetrant craniofacial defects

Genotypea nb Me-PQ fusionc Sy-Ch fusionc Sy shortc
Siblings 611 0% 0% 0%
itga8b1161 (zyg) 129 26% 64% 42%
itga8b1161 (mat+zyg) 54 26% 55% 43%
itga8oz6 41 9% 34% 73%
itga8oz7 18 28% 44% 67%
itga8oz6/oz7 16 38% 31% 78%
itga8oz6/b1161 30 5% 38% 53%
fras1te262 147 19% 57% 68%
a

See Methods for details. “Siblings” includes both wild type and individuals heterozygous for b1161. itga8b1161 (zyg) fish are derived from incross of b1161 heterozygotes; itga8b1161 (mat+zyg) fish from an incross of b1161 homozygotes.

b

n, number of individuals for which both left and right sides of the face were scored for cartilage defects.

c

Fish were labeled with alcian/alizarin-stain to reveal cartilage and bone defects at 6 dpf. Individual defects are shown as the percentage of occurrence per side. Me-PQ fusion = fusion between Meckel's and palatoquadrate cartilages; Sy-Ch fusion = fusion between symplectic and ceratohyal cartilages; Sy short = shortened symplectic cartilage.