Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse

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Figure 6.
Figure 6.

Genomic structure of the genes in the SMCR (A) and in the mouse syntenic region (B). Exons of DKFZp586M1120 are represented by gray boxes; exons of other genes are represented by black boxes. Alternative splicing is observed for RAI1,ATP12, and SMCR7. Dashed lines connecting exons represent the alternative splicing. Exon 10 of DKFZp586M1120is located inside exon 6 of the ATP12 splice variant. Arrows indicate the orientation of transcription. The introns 2 and 3 ofKIAA1820 are not to scale.

This Article

  1. Genome Res. 12: 713-728

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