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Figure 2 | BMC Genomics

Figure 2

From: Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

Figure 2

Genomic structure and alternative splicing of CYFIP1, NIPA2, GOLGA8E, and WHDC1L1 genes. (A) Physical map of CYFIP1 and NIPA2 genes. The two genes share a part of the 3' UTR region deduced from sequence analysis. (B) Confirmation of overlap between BAC 26F2 and 289D12 by Southern blot analysis. DNAs from BAC 26F2 and BAC 289D12 were digested with Eco RI and hybridized with a cDNA probe containing part of the CYFIP1 gene. (C) Alternative splicing and protein isoforms of CYFIP1 gene. (D) Alternative splicing and protein isoforms of NIPA2 gene. (E). Alternative splicing and protein isoforms of GOLGA8E gene. (F). Alternative splicing and protein isoforms of WHDC1L1 gene.

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BMC Genomics

ISSN: 1471-2164

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