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Fig. 1 | Molecular Autism

Fig. 1

From: Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder

Fig. 1

Genomic location of CNVs at the PARK2 locus. Red bars and dark blue bars represent deletions and duplication, respectively, at the PARK2 gene detected in the cases. Light blue bars represent duplication identified in healthy controls. Transcript and genomic coordinates corresponds to human genome Build 37 (hg 19). The A region overlaps with exons 3–4, which corresponds to the UBL and RING0 domain of the Parkin protein. The B region overlaps exon 5, which corresponds to the RING0 domain of the Parkin protein. The C region overlaps with exons 6–7, which corresponds to the RING0 and RING1 domain of the Parkin protein

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