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. 2018 May 9;8:7362. doi: 10.1038/s41598-018-25667-3

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Intron-exon structure of the ociad1/2 genes and comparison of their transcript levels in human tissues and cell lines. (A) Intron-exon structures of the genes coding for OCIAD1 and OCIAD2 in human, mouse and zebra fish. Intron-exon structure for the longest transcript was obtained from the Ensemble database (Accession numbers: ENST00000381473.7, ENSMUST00000031038.10, ENSDART00000103365.4, ENST00000508632.5, ENSMUST00000087195.8 and ENSDART00000164503.1). Colored boxes correspond to exons, grey-color indicates untranslated regions. Black solid lines represent introns. The size of introns and exons in nucleotides is mentioned. Introns are not drawn to scale. Exons coding for the double helical domain of OCIAD proteins have been indicated. (B) Comparison of transcript levels of ociad1 and ociad2 across different human tissues and cell lines as per data obtained from the Vertebrate Alternative Splicing and Transcription Database (VastDB, http://vastdb.crg.eu/).