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. 2014 Aug 21;24(1):128–141. doi: 10.1093/hmg/ddu424

Table 1.

Genotyping of several mutant alleles common in inbred mouse strains did not explain the modifying effect observed in the different Crb1rd8/rd8 homozygous lines

Candidate alleles Crb1rd8/rd8/J C57BL/6 Crb1rd8/rd8(1) C57BL/6 Crb1rd8/rd8(2) C57BL/6J Balb/c 129 S2/Sv
Crb1rd8 (c.3481delC)* 100% (10/10) 100% (7/7) 100% (15/15) 0% (0/4) 0% (0/4) 0% (0/4)
Pde6brd1 (c.1041C>A) 0% (0/10) 0% (0/7) 0% (0/15) 0% (0/4) 0% (0/4) 0% (0/4)
Gnat2 (c.518A>G) 0% (0/8) 0% (0/5) 0% (0/15) 0% (0/3) 0% (0/3) 0% (0/3)
Gnat2Cpfl3 (c.598G>A) 0% (0/10) 0% (0/7) 0% (0/15) 0% (0/4) 0% (0/4) 0% (0/4)
RPE65Leu450/Leu450 or
RPE65Met450/Met450 (c.1348C>A)
100% (10/10)
RPE65Met450
100% (7/7)
RPE65Met450
100% (15/15)
RPE65Met450
100% (4/4)
RPE65Met450
100% (4/4)
RPE65Leu450
100% (4/4)
RPE65Leu450

Percentage and absolute number of the genotyping result for the respective mutant and modifying allele. These results were obtained by DNA sequencing of individual animals from the three homozygous Crb1rd8/rd8/J, C57BL/6 Crb1rd8/rd8(1) and C57BL/6 Crb1rd8/rd8(2) mouse lines (n = 10 each) and from wild-type animals from inbred lines with different genetic backgrounds (C57BL/6J, Balb/c and 129 S2/Sv) that served as controls (n = 4 each). In addition to the represented animals in this table all animals used in this study were genotyped for the Crb1rd8 allele.