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. 2012 Mar 15;139(6):1141–1152. doi: 10.1242/dev.072439

Fig. 2.

Fig. 2.

sdp alleles exhibit lesions in the reck coding sequence. (A) Physical map of the end of chromosome 24. sdp critical region (red line) contained at least four genes; simple sequence length polymorphism (SSLP) markers used for mapping are shown and locations of lesions indicated. (B) Predicted protein product zebrafish reck is 956 amino acids long and has an N-terminal signal sequence and two Kazal motifs. (C) Electropherograms showing each of the reck single nucleotide polymorphisms (SNPs). sdpw12 is a splice site mutation at the exon 9-intron 9 boundary, sdpw13 is a C38R substitution in exon 2, sdpw14 is a W252X substitution in exon 9. (C′) sdpw15 is a large deletion of chromosome 24 encompassing at least 0.4 Mb and including the entire sdp critical region.