pre-miRNA Information | |
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pre-miRNA | hsa-mir-3179-1 |
Genomic Coordinates | chr16: 14901508 - 14901591 |
Description | Homo sapiens miR-3179-1 stem-loop |
Comment | None |
RNA Secondary Structure | |
Associated Diseases | |
pre-miRNA | hsa-mir-3179-2 |
Genomic Coordinates | chr16: 16300159 - 16300242 |
Description | Homo sapiens miR-3179-2 stem-loop |
Comment | None |
RNA Secondary Structure | |
Associated Diseases | |
pre-miRNA | hsa-mir-3179-3 |
Genomic Coordinates | chr16: 18411894 - 18411977 |
Description | Homo sapiens miR-3179-3 stem-loop |
Comment | None |
RNA Secondary Structure | |
Associated Diseases | |
pre-miRNA | hsa-mir-3179-4 |
Genomic Coordinates | chr16: 18494493 - 18494576 |
Description | Homo sapiens miR-3179-4 stem-loop |
Comment | None |
RNA Secondary Structure | |
Associated Diseases |
Mature miRNA Information | ||||||||||||||||
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Mature miRNA | hsa-miR-3179 | |||||||||||||||
Sequence | 52| AGAAGGGGUGAAAUUUAAACGU |73 | |||||||||||||||
Evidence | Experimental | |||||||||||||||
Experiments | Illumina | |||||||||||||||
SNPs in miRNA |
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Putative Targets |
miRNA Expression profile | |
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miRNAs in Extracellular Vesicles |
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Circulating MicroRNA Expression Profiling |
Gene Information | |||||||||||||||||||||
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Gene Symbol | PABPC1L2B | ||||||||||||||||||||
Synonyms | RBM32B | ||||||||||||||||||||
Description | poly(A) binding protein cytoplasmic 1 like 2B | ||||||||||||||||||||
Transcript | NM_001042506 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on PABPC1L2B | |||||||||||||||||||||
3'UTR of PABPC1L2B (miRNA target sites are highlighted) |
>PABPC1L2B|NM_001042506|3'UTR 1 AGACATCCCAGGAGCTAGCCAGCCAGCAGAGCCAAACCTTGGCTCACACCCGGTTTACAACCCCCCACCCCCAGCCCTCC 81 CCCGCCAACCCACCAGCAGTGTATTTATTGTATTGAGAGTGCAGGTCTCTCTCTCTCTCTCTCTCCCCTTCTCTCTCCCC 161 GCTTCCTATTTTCTCCCTCCACCTCTCCTCTCCTTCCCTTCCTCTCCCCCGCCCACCCCCACCAAGGGCGTTGTGAATAA 241 TCTTACTAATCTGTGCCATTTGTAGGTTAAAGGCTGCCTCTTCTCCCTGTGGTTTGGTTTAAAAAGCATTTTCATTCTCT 321 CTTTGTTTACTGCACAGGTGGTACAATTTCATGGTAGAATCATCAGAAAGGAGAAGGATATCAGATGAGGGAAGAAACAA 401 GAGAGTAATTGCTCCCCTGGTCCTACTCCCCAGAGAGAACCACTTTTACCTTTTTGGTGTGCTGCTTTTCCAGGCTCTCT 481 TCTCTCCCTCTCTCTCCTTTGCTCACCCCCACCCCGCCTTCCCTTTTAACACACCGTTATAGAATGGTTCATGTATGTGG 561 TGTTTCTTAACCTGCTTTTTCAGCAACTAAAACCAAACAAAAATCAACCCATTGAACTTCTTTCCATGTTATCAACAGGC 641 TTATGAAATGTCATCTTCAGTGCCTGCAGAGTGCTCCAGTGTATCCGTGGACCTTAACATTTCTGTAATCATTCCCGCAT 721 TGTTGGACATTCAGGTGGTGCCTAGTTCTTTCCCTGTGTTTAAGACCAACATTGCGTGCTCTGTGCTTTGATGAGTGAAT 801 CCTTCCTTGTCAAGCCAAATCTTTGCTAGCATCCCGGTGGTCTCCTTAACTGCGGACTTGCAAGATCCACATATAGACAT 881 TTTAAAGACTTTTCCTGTGTGTTGCCAAAAGGCCCCCTTCATAAGCATTGTACCGATTTGCACTCGTGCCGGCCAGCGCA 961 GCTAGTAAAGAGTATGCCCGTTTCCCCTGCATAGCCTCCTGGTCACTGTAATTGATCGTGTGTGTGCGTGCGTGCGTGTG 1041 TGCATGCGTGTGTGTGTCTTTGTGTGTGTGTCTTGGCCAGCTTGGCGGGCTGCAAAGGGTGTTTCCCTGTCCTCAGTGGT 1121 TTTGCTGCAATCAAACACTGTTTATTACCCCCTTCCCCTGTGCCCACTTCCTGTCCTTTTCCCTGTTGTCAGAAAAATAA 1201 TTCAGCGTCATTGCAGGAAAAAAATAATCACGAAGCAGACAAGTTAACAGAAGAAAATTAATGTCACCAGTAATCATTTC 1281 TGATGATTACTTATACATTCCTGAAACATTTTCATCTGTATCTGCCCTGTATTTTTCATGTGATATATATGTGAAATTAT 1361 TGTATATACTGTTTCAATATCTGCTTTTTCACACAGAAATATATATTATAGACATAGATTTATAGATATTCTTGAACTTT 1441 CATGTCATTAAATATTCTTCTAAAATA Target sites
Provided by authors
Predicted by miRanda
DRVs
SNPs
DRVs & SNPs
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miRNA-target interactions (Predicted by miRanda) |
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SNPs in gene 3'UTRs |
Experimental Support 1 for Functional miRNA-Target Interaction | |||||||
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miRNA:Target | ---- | ||||||
Validation Method |
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Conditions | hESCs (WA-09) | ||||||
Disease | 645974.0 | ||||||
Location of target site | 3'UTR | ||||||
Tools used in this research | TargetScan , miRTarCLIP , Piranha | ||||||
Original Description (Extracted from the article) |
...
"PAR-CLIP data was present in SRR359787. RNA binding protein: AGO2. Condition:4-thiouridine
... - Lipchina I; Elkabetz Y; Hafner M; Sheridan et al., 2011, Genes & development. |
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miRNA-target interactions (Provided by authors) |
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Article |
- Lipchina I; Elkabetz Y; Hafner M; Sheridan et al. - Genes & development, 2011
MicroRNAs are important regulators in many cellular processes, including stem cell self-renewal. Recent studies demonstrated their function as pluripotency factors with the capacity for somatic cell reprogramming. However, their role in human embryonic stem (ES) cells (hESCs) remains poorly understood, partially due to the lack of genome-wide strategies to identify their targets. Here, we performed comprehensive microRNA profiling in hESCs and in purified neural and mesenchymal derivatives. Using a combination of AGO cross-linking and microRNA perturbation experiments, together with computational prediction, we identified the targets of the miR-302/367 cluster, the most abundant microRNAs in hESCs. Functional studies identified novel roles of miR-302/367 in maintaining pluripotency and regulating hESC differentiation. We show that in addition to its role in TGF-beta signaling, miR-302/367 promotes bone morphogenetic protein (BMP) signaling by targeting BMP inhibitors TOB2, DAZAP2, and SLAIN1. This study broadens our understanding of microRNA function in hESCs and is a valuable resource for future studies in this area.
LinkOut: [PMID: 22012620]
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Experimental Support 2 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
|
Conditions | C8166 , TZM-bl |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
PAR-CLIP data was present in GSM1462572. RNA binding protein: AGO2. Condition:C8166 NL4-3
PAR-CLIP data was present in GSM1462574. RNA binding protein: AGO2. Condition:TZM-bl ami BaL
... - Whisnant AW; Bogerd HP; Flores O; Ho P; et al., 2013, mBio. |
Article |
- Whisnant AW; Bogerd HP; Flores O; Ho P; et al. - mBio, 2013
UNLABELLED: The question of how HIV-1 interfaces with cellular microRNA (miRNA) biogenesis and effector mechanisms has been highly controversial. Here, we first used deep sequencing of small RNAs present in two different infected cell lines (TZM-bl and C8166) and two types of primary human cells (CD4(+) peripheral blood mononuclear cells [PBMCs] and macrophages) to unequivocally demonstrate that HIV-1 does not encode any viral miRNAs. Perhaps surprisingly, we also observed that infection of T cells by HIV-1 has only a modest effect on the expression of cellular miRNAs at early times after infection. Comprehensive analysis of miRNA binding to the HIV-1 genome using the photoactivatable ribonucleoside-induced cross-linking and immunoprecipitation (PAR-CLIP) technique revealed several binding sites for cellular miRNAs, a subset of which were shown to be capable of mediating miRNA-mediated repression of gene expression. However, the main finding from this analysis is that HIV-1 transcripts are largely refractory to miRNA binding, most probably due to extensive viral RNA secondary structure. Together, these data demonstrate that HIV-1 neither encodes viral miRNAs nor strongly influences cellular miRNA expression, at least early after infection, and imply that HIV-1 transcripts have evolved to avoid inhibition by preexisting cellular miRNAs by adopting extensive RNA secondary structures that occlude most potential miRNA binding sites. IMPORTANCE: MicroRNAs (miRNAs) are a ubiquitous class of small regulatory RNAs that serve as posttranscriptional regulators of gene expression. Previous work has suggested that HIV-1 might subvert the function of the cellular miRNA machinery by expressing viral miRNAs or by dramatically altering the level of cellular miRNA expression. Using very sensitive approaches, we now demonstrate that neither of these ideas is in fact correct. Moreover, HIV-1 transcripts appear to largely avoid regulation by cellular miRNAs by adopting an extensive RNA secondary structure that occludes the ability of cellular miRNAs to interact with viral mRNAs. Together, these data suggest that HIV-1, rather than seeking to control miRNA function in infected cells, has instead evolved a mechanism to become largely invisible to cellular miRNA effector mechanisms.
LinkOut: [PMID: 23592263]
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Experimental Support 3 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | HEK293/HeLa |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
HITS-CLIP data was present in GSM1067869. RNA binding protein: AGO2. Condition:Ago2 IP-seq (asynchronous cells)
HITS-CLIP data was present in GSM1067870. RNA binding protein: AGO2. Condition:Ago2 IP-seq (mitotic cells)
... - Kishore S; Gruber AR; Jedlinski DJ; Syed et al., 2013, Genome biology. |
Article |
- Kishore S; Gruber AR; Jedlinski DJ; Syed et al. - Genome biology, 2013
BACKGROUND: In recent years, a variety of small RNAs derived from other RNAs with well-known functions such as tRNAs and snoRNAs, have been identified. The functional relevance of these RNAs is largely unknown. To gain insight into the complexity of snoRNA processing and the functional relevance of snoRNA-derived small RNAs, we sequence long and short RNAs, small RNAs that co-precipitate with the Argonaute 2 protein and RNA fragments obtained in photoreactive nucleotide-enhanced crosslinking and immunoprecipitation (PAR-CLIP) of core snoRNA-associated proteins. RESULTS: Analysis of these data sets reveals that many loci in the human genome reproducibly give rise to C/D box-like snoRNAs, whose expression and evolutionary conservation are typically less pronounced relative to the snoRNAs that are currently cataloged. We further find that virtually all C/D box snoRNAs are specifically processed inside the regions of terminal complementarity, retaining in the mature form only 4-5 nucleotides upstream of the C box and 2-5 nucleotides downstream of the D box. Sequencing of the total and Argonaute 2-associated populations of small RNAs reveals that despite their cellular abundance, C/D box-derived small RNAs are not efficiently incorporated into the Ago2 protein. CONCLUSIONS: We conclude that the human genome encodes a large number of snoRNAs that are processed along the canonical pathway and expressed at relatively low levels. Generation of snoRNA-derived processing products with alternative, particularly miRNA-like, functions appears to be uncommon.
LinkOut: [PMID: 23706177]
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Experimental Support 4 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | HEK293S |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
HITS-CLIP data was present in GSM1084065. RNA binding protein: AGO2. Condition:CLIP_emetine_AbnovaAb
... - Karginov FV; Hannon GJ, 2013, Genes & development. |
Article |
- Karginov FV; Hannon GJ - Genes & development, 2013
When adapting to environmental stress, cells attenuate and reprogram their translational output. In part, these altered translation profiles are established through changes in the interactions between RNA-binding proteins and mRNAs. The Argonaute 2 (Ago2)/microRNA (miRNA) machinery has been shown to participate in stress-induced translational up-regulation of a particular mRNA, CAT-1; however, a detailed, transcriptome-wide understanding of the involvement of Ago2 in the process has been lacking. Here, we profiled the overall changes in Ago2-mRNA interactions upon arsenite stress by cross-linking immunoprecipitation (CLIP) followed by high-throughput sequencing (CLIP-seq). Ago2 displayed a significant remodeling of its transcript occupancy, with the majority of 3' untranslated region (UTR) and coding sequence (CDS) sites exhibiting stronger interaction. Interestingly, target sites that were destined for release from Ago2 upon stress were depleted in miRNA complementarity signatures, suggesting an alternative mode of interaction. To compare the changes in Ago2-binding patterns across transcripts with changes in their translational states, we measured mRNA profiles on ribosome/polysome gradients by RNA sequencing (RNA-seq). Increased Ago2 occupancy correlated with stronger repression of translation for those mRNAs, as evidenced by a shift toward lighter gradient fractions upon stress, while release of Ago2 was associated with the limited number of transcripts that remained translated. Taken together, these data point to a role for Ago2 and the mammalian miRNAs in mediating the translational component of the stress response.
LinkOut: [PMID: 23824327]
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Experimental Support 5 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | MCF7 |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
PAR-CLIP data was present in SRR1045082. RNA binding protein: AGO2. Condition:Untreated
... - Farazi TA; Ten Hoeve JJ; Brown M; et al., 2014, Genome biology. |
Article |
- Farazi TA; Ten Hoeve JJ; Brown M; et al. - Genome biology, 2014
BACKGROUND: Various microRNAs (miRNAs) are up- or downregulated in tumors. However, the repression of cognate miRNA targets responsible for the phenotypic effects of this dysregulation in patients remains largely unexplored. To define miRNA targets and associated pathways, together with their relationship to outcome in breast cancer, we integrated patient-paired miRNA-mRNA expression data with a set of validated miRNA targets and pathway inference. RESULTS: To generate a biochemically-validated set of miRNA-binding sites, we performed argonaute-2 photoactivatable-ribonucleoside-enhanced crosslinking and immunoprecipitation (AGO2-PAR-CLIP) in MCF7 cells. We then defined putative miRNA-target interactions using a computational model, which ranked and selected additional TargetScan-predicted interactions based on features of our AGO2-PAR-CLIP binding-site data. We subselected modeled interactions according to the abundance of their constituent miRNA and mRNA transcripts in tumors, and we took advantage of the variability of miRNA expression within molecular subtypes to detect miRNA repression. Interestingly, our data suggest that miRNA families control subtype-specific pathways; for example, miR-17, miR-19a, miR-25, and miR-200b show high miRNA regulatory activity in the triple-negative, basal-like subtype, whereas miR-22 and miR-24 do so in the HER2 subtype. An independent dataset validated our findings for miR-17 and miR-25, and showed a correlation between the expression levels of miR-182 targets and overall patient survival. Pathway analysis associated miR-17, miR-19a, and miR-200b with leukocyte transendothelial migration. CONCLUSIONS: We combined PAR-CLIP data with patient expression data to predict regulatory miRNAs, revealing potential therapeutic targets and prognostic markers in breast cancer.
LinkOut: [PMID: 24398324]
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Experimental Support 6 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | HCT116 |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
PAR-CLIP data was present in ERX177612. RNA binding protein: AGO2. Condition:p53_V_AGO_CLIP_3_2
PAR-CLIP data was present in ERX177599. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_2_1
PAR-CLIP data was present in ERX177622. RNA binding protein: AGO2. Condition:KO_V_AGO_CLIP_3_12
PAR-CLIP data was present in ERX177634. RNA binding protein: AGO2. Condition:KO_V_AGO_CLIP_4_12
PAR-CLIP data was present in ERX177600. RNA binding protein: AGO2. Condition:p53_V_Ago_CLIP_2_2
PAR-CLIP data was present in ERX177611. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_3_1
PAR-CLIP data was present in ERX177623. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_4_1
... - Krell J; Stebbing J; Carissimi C; Dabrowska et al., 2016, Genome research. |
Article |
- Krell J; Stebbing J; Carissimi C; Dabrowska et al. - Genome research, 2016
DNA damage activates TP53-regulated surveillance mechanisms that are crucial in suppressing tumorigenesis. TP53 orchestrates these responses directly by transcriptionally modulating genes, including microRNAs (miRNAs), and by regulating miRNA biogenesis through interacting with the DROSHA complex. However, whether the association between miRNAs and AGO2 is regulated following DNA damage is not yet known. Here, we show that, following DNA damage, TP53 interacts with AGO2 to induce or reduce AGO2's association of a subset of miRNAs, including multiple let-7 family members. Furthermore, we show that specific mutations in TP53 decrease rather than increase the association of let-7 family miRNAs, reducing their activity without preventing TP53 from interacting with AGO2. This is consistent with the oncogenic properties of these mutants. Using AGO2 RIP-seq and PAR-CLIP-seq, we show that the DNA damage-induced increase in binding of let-7 family members to the RISC complex is functional. We unambiguously determine the global miRNA-mRNA interaction networks involved in the DNA damage response, validating them through the identification of miRNA-target chimeras formed by endogenous ligation reactions. We find that the target complementary region of the let-7 seed tends to have highly fixed positions and more variable ones. Additionally, we observe that miRNAs, whose cellular abundance or differential association with AGO2 is regulated by TP53, are involved in an intricate network of regulatory feedback and feedforward circuits. TP53-mediated regulation of AGO2-miRNA interaction represents a new mechanism of miRNA regulation in carcinogenesis.
LinkOut: [PMID: 26701625]
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Experimental Support 7 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | Prostate Tissue |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
PAR-CLIP data was present in SRX1760618. RNA binding protein: AGO2. Condition:AGO-CLIP-PC3_B
PAR-CLIP data was present in SRX1760616. RNA binding protein: AGO2. Condition:AGO-CLIP-PC3_A
PAR-CLIP data was present in SRX1760637. RNA binding protein: AGO2. Condition:AGO-CLIP-DU145_A
PAR-CLIP data was present in SRX1760628. RNA binding protein: AGO2. Condition:AGO-CLIP-LAPC4_B
PAR-CLIP data was present in SRX1760630. RNA binding protein: AGO2. Condition:AGO-CLIP-22RV1_A
... - Hamilton MP; Rajapakshe KI; Bader DA; Cerne et al., 2016, Neoplasia (New York, N.Y.). |
Article |
- Hamilton MP; Rajapakshe KI; Bader DA; Cerne et al. - Neoplasia (New York, N.Y.), 2016
MicroRNA (miRNA) deregulation in prostate cancer (PCa) contributes to PCa initiation and metastatic progression. To comprehensively define the cancer-associated changes in miRNA targeting and function in commonly studied models of PCa, we performed photoactivatable ribonucleoside-enhanced cross-linking immunoprecipitation of the Argonaute protein in a panel of PCa cell lines modeling different stages of PCa progression. Using this comprehensive catalogue of miRNA targets, we analyzed miRNA targeting on known drivers of PCa and examined tissue-specific and stage-specific pathway targeting by miRNAs. We found that androgen receptor is the most frequently targeted PCa oncogene and that miR-148a targets the largest number of known PCa drivers. Globally, tissue-specific and stage-specific changes in miRNA targeting are driven by homeostatic response to active oncogenic pathways. Our findings indicate that, even in advanced PCa, the miRNA pool adapts to regulate continuing alterations in the cancer genome to balance oncogenic molecular changes. These findings are important because they are the first to globally characterize miRNA changes in PCa and demonstrate how the miRNA target spectrum responds to staged tumorigenesis.
LinkOut: [PMID: 27292025]
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CLIP-seq Support 1 for dataset GSM4903829 | |
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Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | Human neurons / CTLTD_shCTL_a |
Location of target site | NM_001042506 | 3UTR | GGCCCCCUUCAUAAG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE161238 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 for dataset GSM4903830 | |
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Method / RBP | HITS-CLIP / AGO |
Cell line / Condition | Human neurons / CTLTD_shCTL_b |
Location of target site | NM_001042506 | 3UTR | GGCCCCCUUCAUAAG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Accession Series | GSE161238 |
CLIP-seq Viewer | Link |
CLIP-seq Support 3 for dataset GSM1067869 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293/HeLa / Ago2 IP-seq (asynchronous cells) |
Location of target site | ENST00000373521.2 | 3UTR | UCUCUCUCUCUCUCUCUCCCC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23706177 / GSE43666 |
CLIP-seq Viewer | Link |
CLIP-seq Support 4 for dataset GSM1067870 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293/HeLa / Ago2 IP-seq (mitotic cells) |
Location of target site | ENST00000373521.2 | 3UTR | UCUCUCUCUCUCUCUCUCCCC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23706177 / GSE43666 |
CLIP-seq Viewer | Link |
CLIP-seq Support 5 for dataset GSM1084065 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293S / CLIP_emetine_AbnovaAb |
Location of target site | ENST00000373521.2 | 3UTR | UGCAGGUCUCUCUCUCUCUCUCUCUC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23824327 / GSE44404 |
CLIP-seq Viewer | Link |
CLIP-seq Support 6 for dataset SRR359787 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | hESCs (WA-09) / 4-thiouridine, RNase T1 |
Location of target site | ENST00000373521.2 | 3UTR | CUCUCUCUCUCUCUCUCUCCCCUUCUC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 22012620 / SRX103431 |
CLIP-seq Viewer | Link |
CLIP-seq Support 7 for dataset SRR1045082 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | MCF7 / Untreated |
Location of target site | ENST00000373521.2 | 3UTR | UCUCUCUCUCUCUCUCUCUCCCCUUCUC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 24398324 / SRX388831 |
CLIP-seq Viewer | Link |
CLIP-seq Support 8 for dataset GSM1462572 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | C8166 / C8166 NL4-3 |
Location of target site | ENST00000373521.2 | 3UTR | CUCUCUCUCUCUCUCUCUCCCCUUCU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23592263 / GSE59944 |
CLIP-seq Viewer | Link |
CLIP-seq Support 9 for dataset GSM1462574 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | TZM-bl / TZM-bl ami BaL |
Location of target site | ENST00000373521.2 | 3UTR | CUCUCUCUCUCUCUCUCCCC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23592263 / GSE59944 |
CLIP-seq Viewer | Link |
MiRNA-Target Expression Profile | |||||||
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MiRNA-Target Expression Profile (TCGA) | |||||||||||||||||||||
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ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT102087 | GIGYF1 | GRB10 interacting GYF protein 1 | 2 | 4 | ||||||||
MIRT110061 | OGT | O-linked N-acetylglucosamine (GlcNAc) transferase | 2 | 6 | ||||||||
MIRT112198 | BTG2 | BTG anti-proliferation factor 2 | 2 | 2 | ||||||||
MIRT117668 | SCAMP4 | secretory carrier membrane protein 4 | 2 | 2 | ||||||||
MIRT146657 | MINK1 | misshapen like kinase 1 | 2 | 2 | ||||||||
MIRT175505 | ZBTB33 | zinc finger and BTB domain containing 33 | 2 | 4 | ||||||||
MIRT180535 | TXNIP | thioredoxin interacting protein | 2 | 2 | ||||||||
MIRT190624 | BCL2L2-PABPN1 | BCL2L2-PABPN1 readthrough | 2 | 2 | ||||||||
MIRT190650 | PABPN1 | poly(A) binding protein nuclear 1 | 2 | 2 | ||||||||
MIRT366902 | NONO | non-POU domain containing octamer binding | 2 | 2 | ||||||||
MIRT443554 | ZFP3 | ZFP3 zinc finger protein | 2 | 2 | ||||||||
MIRT445953 | MLLT11 | MLLT11, transcription factor 7 cofactor | 2 | 2 | ||||||||
MIRT446042 | HMCN1 | hemicentin 1 | 2 | 2 | ||||||||
MIRT447968 | MSH6 | mutS homolog 6 | 2 | 2 | ||||||||
MIRT448634 | ONECUT1 | one cut homeobox 1 | 2 | 2 | ||||||||
MIRT449316 | MRO | maestro | 2 | 2 | ||||||||
MIRT451380 | C19orf43 | telomerase RNA component interacting RNase | 2 | 2 | ||||||||
MIRT451547 | CIAPIN1 | cytokine induced apoptosis inhibitor 1 | 2 | 2 | ||||||||
MIRT451807 | CDCA3 | cell division cycle associated 3 | 2 | 4 | ||||||||
MIRT451916 | ILK | integrin linked kinase | 2 | 2 | ||||||||
MIRT451938 | TMPRSS5 | transmembrane protease, serine 5 | 2 | 2 | ||||||||
MIRT452189 | KIAA1456 | KIAA1456 | 2 | 2 | ||||||||
MIRT452498 | HMGXB3 | HMG-box containing 3 | 2 | 2 | ||||||||
MIRT452548 | ZNF467 | zinc finger protein 467 | 2 | 2 | ||||||||
MIRT453844 | SDK1 | sidekick cell adhesion molecule 1 | 2 | 2 | ||||||||
MIRT454515 | ZFYVE27 | zinc finger FYVE-type containing 27 | 2 | 2 | ||||||||
MIRT455363 | KDM5C | lysine demethylase 5C | 2 | 2 | ||||||||
MIRT455455 | EPB41L4B | erythrocyte membrane protein band 4.1 like 4B | 2 | 2 | ||||||||
MIRT455628 | PABPC1L2B | poly(A) binding protein cytoplasmic 1 like 2B | 2 | 10 | ||||||||
MIRT455639 | PABPC1L2A | poly(A) binding protein cytoplasmic 1 like 2A | 2 | 10 | ||||||||
MIRT455690 | GLO1 | glyoxalase I | 2 | 2 | ||||||||
MIRT456300 | ASH1L | ASH1 like histone lysine methyltransferase | 2 | 2 | ||||||||
MIRT456784 | MTHFSD | methenyltetrahydrofolate synthetase domain containing | 2 | 2 | ||||||||
MIRT456819 | PIGP | phosphatidylinositol glycan anchor biosynthesis class P | 2 | 2 | ||||||||
MIRT457566 | ZNF34 | zinc finger protein 34 | 2 | 2 | ||||||||
MIRT457604 | IDS | iduronate 2-sulfatase | 2 | 2 | ||||||||
MIRT458236 | NXPH3 | neurexophilin 3 | 2 | 2 | ||||||||
MIRT458313 | TNFAIP8L3 | TNF alpha induced protein 8 like 3 | 2 | 2 | ||||||||
MIRT458350 | NOC2L | NOC2 like nucleolar associated transcriptional repressor | 2 | 2 | ||||||||
MIRT458670 | GPR35 | G protein-coupled receptor 35 | 2 | 2 | ||||||||
MIRT459675 | VPS37C | VPS37C, ESCRT-I subunit | 2 | 2 | ||||||||
MIRT461126 | RAB36 | RAB36, member RAS oncogene family | 2 | 2 | ||||||||
MIRT461918 | NECAB3 | N-terminal EF-hand calcium binding protein 3 | 2 | 2 | ||||||||
MIRT462301 | PPM1H | protein phosphatase, Mg2+/Mn2+ dependent 1H | 2 | 2 | ||||||||
MIRT463520 | ZBTB7B | zinc finger and BTB domain containing 7B | 2 | 2 | ||||||||
MIRT464378 | URM1 | ubiquitin related modifier 1 | 2 | 2 | ||||||||
MIRT464614 | UBE4B | ubiquitination factor E4B | 2 | 2 | ||||||||
MIRT464711 | UBE2V1 | ubiquitin conjugating enzyme E2 V1 | 2 | 2 | ||||||||
MIRT465520 | PRICKLE4 | prickle planar cell polarity protein 4 | 2 | 2 | ||||||||
MIRT465974 | TMEM189-UBE2V1 | TMEM189-UBE2V1 readthrough | 2 | 2 | ||||||||
MIRT466058 | TMEM189 | transmembrane protein 189 | 2 | 2 | ||||||||
MIRT466548 | TBL1XR1 | transducin beta like 1 X-linked receptor 1 | 2 | 2 | ||||||||
MIRT466647 | TAGLN2 | transgelin 2 | 2 | 2 | ||||||||
MIRT467357 | SP2 | Sp2 transcription factor | 2 | 2 | ||||||||
MIRT468744 | SDC2 | syndecan 2 | 2 | 2 | ||||||||
MIRT470244 | PRRC2A | proline rich coiled-coil 2A | 2 | 2 | ||||||||
MIRT471426 | PDIA6 | protein disulfide isomerase family A member 6 | 2 | 2 | ||||||||
MIRT471732 | OTUB1 | OTU deubiquitinase, ubiquitin aldehyde binding 1 | 2 | 2 | ||||||||
MIRT472190 | NHP2L1 | small nuclear ribonucleoprotein 13 | 2 | 2 | ||||||||
MIRT472450 | NAV2 | neuron navigator 2 | 2 | 6 | ||||||||
MIRT474563 | KLHDC3 | kelch domain containing 3 | 2 | 2 | ||||||||
MIRT474936 | KCTD15 | potassium channel tetramerization domain containing 15 | 2 | 2 | ||||||||
MIRT475165 | IP6K1 | inositol hexakisphosphate kinase 1 | 2 | 2 | ||||||||
MIRT475399 | ICMT | isoprenylcysteine carboxyl methyltransferase | 2 | 4 | ||||||||
MIRT475426 | ICK | intestinal cell kinase | 2 | 2 | ||||||||
MIRT477090 | FAM168A | family with sequence similarity 168 member A | 2 | 2 | ||||||||
MIRT478458 | DAB2 | DAB2, clathrin adaptor protein | 2 | 2 | ||||||||
MIRT478953 | COX15 | COX15, cytochrome c oxidase assembly homolog | 2 | 2 | ||||||||
MIRT480096 | CALR | calreticulin | 2 | 2 | ||||||||
MIRT481924 | ANKRD33B | ankyrin repeat domain 33B | 2 | 2 | ||||||||
MIRT483217 | APOA1 | apolipoprotein A1 | 2 | 6 | ||||||||
MIRT483882 | TGIF1 | TGFB induced factor homeobox 1 | 2 | 2 | ||||||||
MIRT483923 | SPSB1 | splA/ryanodine receptor domain and SOCS box containing 1 | 2 | 2 | ||||||||
MIRT483942 | LENG8 | leukocyte receptor cluster member 8 | 2 | 4 | ||||||||
MIRT484209 | SUMO1 | small ubiquitin-like modifier 1 | 2 | 2 | ||||||||
MIRT484512 | SYT7 | synaptotagmin 7 | 2 | 2 | ||||||||
MIRT484709 | RNF11 | ring finger protein 11 | 2 | 2 | ||||||||
MIRT485356 | MYO1C | myosin IC | 2 | 4 | ||||||||
MIRT485615 | FOSL1 | FOS like 1, AP-1 transcription factor subunit | 2 | 4 | ||||||||
MIRT486584 | ZNF619 | zinc finger protein 619 | 2 | 2 | ||||||||
MIRT487013 | C2orf82 | chromosome 2 open reading frame 82 | 2 | 2 | ||||||||
MIRT487621 | C20orf96 | chromosome 20 open reading frame 96 | 2 | 2 | ||||||||
MIRT487801 | GPR20 | G protein-coupled receptor 20 | 2 | 4 | ||||||||
MIRT488134 | GPR107 | G protein-coupled receptor 107 | 2 | 2 | ||||||||
MIRT488773 | FXYD1 | FXYD domain containing ion transport regulator 1 | 2 | 2 | ||||||||
MIRT488854 | UBTF | upstream binding transcription factor, RNA polymerase I | 2 | 2 | ||||||||
MIRT489783 | GRINA | glutamate ionotropic receptor NMDA type subunit associated protein 1 | 2 | 2 | ||||||||
MIRT490102 | FN3K | fructosamine 3 kinase | 2 | 2 | ||||||||
MIRT490389 | LHFPL3 | LHFPL tetraspan subfamily member 3 | 2 | 2 | ||||||||
MIRT490434 | MYL9 | myosin light chain 9 | 2 | 2 | ||||||||
MIRT490451 | GLUD1 | glutamate dehydrogenase 1 | 2 | 2 | ||||||||
MIRT490880 | OSBP | oxysterol binding protein | 2 | 2 | ||||||||
MIRT491037 | ALPK3 | alpha kinase 3 | 2 | 2 | ||||||||
MIRT491250 | HCN2 | hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 | 2 | 2 | ||||||||
MIRT491748 | SEMA3F | semaphorin 3F | 2 | 2 | ||||||||
MIRT492235 | SLC48A1 | solute carrier family 48 member 1 | 2 | 2 | ||||||||
MIRT492490 | RAPGEF1 | Rap guanine nucleotide exchange factor 1 | 2 | 2 | ||||||||
MIRT492505 | RANBP10 | RAN binding protein 10 | 2 | 4 | ||||||||
MIRT492773 | PDGFB | platelet derived growth factor subunit B | 2 | 2 | ||||||||
MIRT492922 | NFAT5 | nuclear factor of activated T-cells 5 | 2 | 2 | ||||||||
MIRT493459 | ITFG3 | family with sequence similarity 234 member A | 2 | 2 | ||||||||
MIRT493654 | HDLBP | high density lipoprotein binding protein | 2 | 2 | ||||||||
MIRT494011 | DUSP9 | dual specificity phosphatase 9 | 2 | 2 | ||||||||
MIRT499412 | PLCG2 | phospholipase C gamma 2 | 2 | 4 | ||||||||
MIRT499552 | C15orf43 | telomere repeat binding bouquet formation protein 2 | 2 | 2 | ||||||||
MIRT501836 | NCOA2 | nuclear receptor coactivator 2 | 2 | 2 | ||||||||
MIRT501950 | MAT2A | methionine adenosyltransferase 2A | 2 | 10 | ||||||||
MIRT504066 | KCTD12 | potassium channel tetramerization domain containing 12 | 2 | 4 | ||||||||
MIRT504509 | PPP1R9B | protein phosphatase 1 regulatory subunit 9B | 2 | 2 | ||||||||
MIRT508466 | HOXB6 | homeobox B6 | 2 | 4 | ||||||||
MIRT512373 | CPM | carboxypeptidase M | 2 | 2 | ||||||||
MIRT513578 | EVX1 | even-skipped homeobox 1 | 2 | 2 | ||||||||
MIRT517763 | ZNF366 | zinc finger protein 366 | 2 | 4 | ||||||||
MIRT519773 | ZNF354B | zinc finger protein 354B | 2 | 8 | ||||||||
MIRT523568 | GGCX | gamma-glutamyl carboxylase | 2 | 4 | ||||||||
MIRT532802 | CLDN11 | claudin 11 | 2 | 2 | ||||||||
MIRT544299 | TSPYL1 | TSPY like 1 | 2 | 2 | ||||||||
MIRT544862 | MYH2 | myosin heavy chain 2 | 2 | 4 | ||||||||
MIRT556731 | KLHL15 | kelch like family member 15 | 2 | 4 | ||||||||
MIRT564347 | AKR1B10 | aldo-keto reductase family 1 member B10 | 2 | 2 | ||||||||
MIRT568924 | SMCR8 | Smith-Magenis syndrome chromosome region, candidate 8 | 2 | 2 | ||||||||
MIRT569012 | CXorf36 | chromosome X open reading frame 36 | 2 | 2 | ||||||||
MIRT569256 | FAM129B | family with sequence similarity 129 member B | 2 | 2 | ||||||||
MIRT569591 | PRELP | proline and arginine rich end leucine rich repeat protein | 2 | 2 | ||||||||
MIRT569779 | SAMD14 | sterile alpha motif domain containing 14 | 2 | 2 | ||||||||
MIRT570034 | FAM228A | family with sequence similarity 228 member A | 2 | 2 | ||||||||
MIRT573803 | FRMPD4 | FERM and PDZ domain containing 4 | 2 | 2 | ||||||||
MIRT574190 | ZNF264 | zinc finger protein 264 | 2 | 2 | ||||||||
MIRT576153 | Hmox1 | heme oxygenase 1 | 2 | 2 | ||||||||
MIRT611311 | CA8 | carbonic anhydrase 8 | 2 | 4 | ||||||||
MIRT673429 | APAF1 | apoptotic peptidase activating factor 1 | 2 | 2 | ||||||||
MIRT674976 | SH3BP2 | SH3 domain binding protein 2 | 2 | 2 | ||||||||
MIRT692712 | MEAF6 | MYST/Esa1 associated factor 6 | 2 | 2 |
miRNA-Drug Resistance Associations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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