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. 2020 Apr 30;77(20):4069–4080. doi: 10.1007/s00018-020-03526-7

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© The Author(s) 2020, corrected publication 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Map of microRNA sequences on human X chromosome. Information about validated miRNA sequence position is based on Ensembl and miRBase databases. On the left, chromosome bands are indicated and on the right, the miRNA names, simplified by eliminating « hsa-miR- » and indicated only by the number. Some miRNAs are intragenic and the host gene is indicated (name of host gene). Several miRNAs are clustered (within 10 kbp) and are shown on the same line separated by ‘,’, with the exception of miR-514b (*) that is located within 10.3 kbp of adjacent cluster; miRNA name is repeated when it can be considered belonging to different clusters. Some miRNAs are mainly involved in immunity ( ), cancer ( ) and cardiovascular homeostasis ( ), as detailed in the text. LOC10798567, uncharacterized non-coding RNA; CTPS2, CTP synthase 2; CLCN5, chloride voltage-gated channel 5; HUWE1, HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1; EDA, ectodysplasin A; FTX, FTX transcript, XIST regulator; CHM, CHM Rab escort protein; HTR2C, 5-hydroxytryptamine receptor 2C; WDR44, WD repeat domain 44; SEPTIN6, septin 6; MIR503HG, miR-503 host gene; FGF13, fibroblast growth factor 13; LOC105373347, periphilin-1-like; LOC101928863, uncharacterized non-coding RNA; GABRE, gamma-aminobutyric acid type A receptor epsilon subunit; GABRA3, gamma-aminobutyric acid type A receptor alpha3 subunit; SNORA36A, smal nucleolar RNA, H/ACA box 36A; DKC, dyskerin pseudouridine synthase 1.

The figure was inspired by Pinheiro et al. (2011) [35]

Inline graphic — Map of microRNA sequences on human X chromosome. Information about validated miRNA sequence position is based on Ensembl and miRBase databases. On the left, chromosome bands are indicated and on the right, the miRNA names, simplified by eliminating « hsa-miR- » and indicated only by the number. Some miRNAs are intragenic and the host gene is indicated (name of host gene). Several miRNAs are clustered (within 10 kbp) and are shown on the same line separated by ‘,’, with the exception of miR-514b (*) that is located within 10.3 kbp of adjacent cluster; miRNA name is repeated when it can be considered belonging to different clusters. Some miRNAs are mainly involved in immunity ( ), cancer ( ) and cardiovascular homeostasis ( ), as detailed in the text. LOC10798567, uncharacterized non-coding RNA; CTPS2, CTP synthase 2; CLCN5, chloride voltage-gated channel 5; HUWE1, HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1; EDA, ectodysplasin A; FTX, FTX transcript, XIST regulator; CHM, CHM Rab escort protein; HTR2C, 5-hydroxytryptamine receptor 2C; WDR44, WD repeat domain 44; SEPTIN6, septin 6; MIR503HG, miR-503 host gene; FGF13, fibroblast growth factor 13; LOC105373347, periphilin-1-like; LOC101928863, uncharacterized non-coding RNA; GABRE, gamma-aminobutyric acid type A receptor epsilon subunit; GABRA3, gamma-aminobutyric acid type A receptor alpha3 subunit; SNORA36A, smal nucleolar RNA, H/ACA box 36A; DKC, dyskerin pseudouridine synthase 1.

The figure was inspired by Pinheiro et al. (2011) [35]