pre-miRNA Information | |
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pre-miRNA | hsa-mir-124-1 |
Genomic Coordinates | chr8: 9903388 - 9903472 |
Description | Homo sapiens miR-124-1 stem-loop |
Comment | miR-124 was first identified by cloning studies in mouse . The 5' end of the miRNA may be offset with respect to previous annotations. |
RNA Secondary Structure | |
Associated Diseases | |
pre-miRNA | hsa-mir-124-2 |
Genomic Coordinates | chr8: 64379149 - 64379257 |
Description | Homo sapiens miR-124-2 stem-loop |
Comment | miR-124 was first identified by cloning studies in mouse . The 5' end of the miRNA may be offset with respect to previous annotations. |
RNA Secondary Structure | |
Associated Diseases | |
pre-miRNA | hsa-mir-124-3 |
Genomic Coordinates | chr20: 63178500 - 63178586 |
Description | Homo sapiens miR-124-3 stem-loop |
Comment | miR-124 was first identified by cloning studies in mouse . The 5' end of the miRNA may be offset with respect to previous annotations. |
RNA Secondary Structure | |
Associated Diseases |
Mature miRNA Information | |||||||||||||||||||||||||||||||
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Mature miRNA | hsa-miR-124-5p | ||||||||||||||||||||||||||||||
Sequence | 14| CGUGUUCACAGCGGACCUUGAU |35 | ||||||||||||||||||||||||||||||
Evidence | Experimental | ||||||||||||||||||||||||||||||
Experiments | Cloned | ||||||||||||||||||||||||||||||
Editing Events in miRNAs |
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SNPs in miRNA |
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Putative Targets |
miRNA Expression profile | |
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Human miRNA Tissue Atlas | |
miRNAs in Extracellular Vesicles |
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Circulating MicroRNA Expression Profiling |
Biomarker Information |
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Gene Information | |||||||||||||||||||||
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Gene Symbol | NABP1 | ||||||||||||||||||||
Synonyms | OBFC2A, SOSS-B2, SSB2 | ||||||||||||||||||||
Description | nucleic acid binding protein 1 | ||||||||||||||||||||
Transcript | NM_001031716 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on NABP1 | |||||||||||||||||||||
3'UTR of NABP1 (miRNA target sites are highlighted) |
>NABP1|NM_001031716|3'UTR 1 CCTATGCTAAATACTCATGTGTAGTTTTTATACTACATGCCCTACTTGAACACTTATTGCACTTTTATTTATTGTTAACT 81 GTGAAAAGTACGTCCTTTATTGGGTTTCCTTTTATATTCTTGGTTTGTTAAGAAGAATGGTTTGTTTTTATAGCAAAACT 161 GTTAAGCTGCTCGAGTCTCCTGTTGAAGAATGGGAACACTGAAAAGTAGGGGCATTTATTTTTAGAGTAAAAAGATTATT 241 GGATAGCCTTTAAAAAACCTGCACCCATTTCATGGGTGAGTTACTTAAGACATCAGCTTTATAGCCTCTATGAGTCTATC 321 TTCTGTATAAGTTTTGTAATATTTAACATAAGGCTTAATGGGAGATGTTCTTTTGTCTTGTATTCAGATATTGCCAACTA 401 AAGCAATAACCATCAAAAAACACAAGAACTTGTCAATGCTAGCAGTAATTTTTGAGTGTTTGTGGCTCTCGGAATGATTG 481 ACTTCGTTCAGTGACTACTATTAAGATTTTCCAAGGACTGACTCATCCCAAATTTTTGTTGTATTACCAAAAAAACAGAT 561 TCCTTATCAGAATTTGGAATAGAATGTGATCTCTATTGCAACAAGTAATTTTAAAAGAAAGCTACATTTATTTTAGAGTA 641 GTGCTCCTAACATGTATTATCAACTTTGTGGATTACATTGGAGGAAAATTTAAAACTGGGGCCTTGAATATTTATTTTTT 721 GAAACTACCATGTTAAATACTGAAGTATAATTTGGGGGAGTTATAAAGTTATGATAAACATTCATCTGATTATTTTAAAC 801 AATAGTTGTGGTAGATAAACATACTGGAGGTGAGTCAAATTGAATTCATATAGTAACATGCAGTCTGAAGTCCTAGTTAC 881 TTAATAGGTACTCAGCCTGGAGTGAAAATCCTGGGTACTGACTTTGAGAGGAGTGAGTGTGCATGTTGTCAAAGTTTCTG 961 AACACAGTTCACATAGCCTTATTAGCAAAAGTTTTAAGAAATGGCTCTATCAAAGAAGCAATTGCAGCTTTATTCAGAAA 1041 TATAAAAGTGGAATTTATGTACATGTCATAAGTGGTACCCACTTCCCCTTTTTACTGTAGGGTGGATAACTCTTAGGATT 1121 TAACTCTTTGAATATTATCTCTTGAATAAAGCATGTGTTAATGTTAACAAACCTACGTAATTTTTGCCCTTTCAATGACT 1201 TACAGTGGAGAGCCAGTACATCTTAACTACTGTTGTAGTGATGGTATCAACCTCATGGTTACTTAGCTCTGCATTTGTTG 1281 CTTTGTTTTTTTTCCACTTCAAATCACAAAATAAGTAGATTTTGTTTTCTGAAAACTCCATAGCATTTGAATACAAAAAG 1361 TTGTGCCAGATTGTTTGCCCTAATTCACTGTGTTTAACAAATATTTCAGTACACACTATGTATTAGGCACTGTGTGGAAA 1441 GTGTTAAGGGGTAGACAAAATACCGAATAATCTCCACAAGTTTATTTGTGGTCTATAGTACTTTTGTAACTGGGGTTACA 1521 AAAATTATAGAAATTTTTTTCCTTTGTTCATATGCATATTCATGATTATAATTTGGCTTTGTTTGTGATTAATGTTTTCT 1601 TAAGATTTTCACATTATAGAATACCTCAAAAGAAGTTGTCTAAGGACTGGGATAGAGAGTATGTTTCATAAAATTGTAGA 1681 TGTTTAGAATTTTTAAAAACCCTACAAATTAGTATATGATTGTTTTATATAAGTAAGATAGGAGCAACACTTTAAATTAT 1761 TTGTGGGAGAATACAGCATTAAAGGTGATTTTAAAAGAAAAAAATTTGGAATTTTAGAAAATTTAAATGCTGTCAGGTAT 1841 GGAATGCTGGGCTTCCAATCCTGGCCTCATTGTCTCCTCACCTGTGATGTTGGATGAGTTATTACACTTGAAATGTCTTT 1921 AAGCCTTAGGTTCCACAAGTATGAAAACAAGTAAGTAACAGTATCCTTTCTAGACTTGTTTAAGATTTCCATGTAAGTAA 2001 TTATAATGACTTCTGACACATAATAATGTCGTCTTATACCCCAACAGTAGGAAAAAAATGCAGAATTCAGTATGAAAGTA 2081 TTGTTACCCTTTAACACAGTGGTCCCCAACCTTTTTGGCACCAGAGACCAGTCTCCTGGAAGACAGTTTTTCCGTGGGAT 2161 CGGGGGATGGTTTTGGGATGAAACTGTTCCACCTCAGGTCATCAGTCATTAGTTAGATTCTCATAAGGAGCGTGCAACCT 2241 CAATCCCTTGCATACTCATTTCACAATAGGGTTCATGCTCCTATGAGAATCTAATGCCACCACTCATCTGACAGGAGGTG 2321 GAGCTCAGGCAGTAAGTCTCCCTCGCCCGCCACTCACCTGCTGGGCGTTCCTGTTCCTAGCAGGCCAGAATTGATACTGA 2401 TCTAGGGGTTGGGGACCCCTGCTTAACATGTTGAGATTAAATGGAGAAAGACTTAAGCTTTTACTTTTGTGATTGACACT 2481 TGCTTCAATAATGTAACCTTGTTCTGTGTTTTTATCATTTATTAACAAATTTCTTTTTTCTTAAGGGAAGCCTCCAAAAT 2561 CAAAGAAAAGTGAGTTACAATCCATAATGAATATTTGCCTTACCAGCCTACTGGAACACATTCATCAAGAACTTAAGAGG 2641 AAGAAAGTTTTCTGCCTTCCTCCTTCCTAGTGCTCTCAGCTATCAACTTTGAAATAAGTTTAAACAACACCTACTGAAAA 2721 CAAAAACCACTTAGTATAAAAATATCCCCCACCAAAAAAAAAAAAAAAAAA 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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DRVs in gene 3'UTRs | |||||||||||||||||||||
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 | HEK293 |
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 GSM545212. RNA binding protein: AGO1. Condition:Control
PAR-CLIP data was present in GSM545214. RNA binding protein: AGO3. Condition:Control
PAR-CLIP data was present in GSM545217. RNA binding protein: AGO2. Condition:miR-7 transfection
... - Hafner M; Landthaler M; Burger L; Khorshid et al., 2010, Cell. |
Article |
- Hafner M; Landthaler M; Burger L; Khorshid et al. - Cell, 2010
RNA transcripts are subject to posttranscriptional gene regulation involving hundreds of RNA-binding proteins (RBPs) and microRNA-containing ribonucleoprotein complexes (miRNPs) expressed in a cell-type dependent fashion. We developed a cell-based crosslinking approach to determine at high resolution and transcriptome-wide the binding sites of cellular RBPs and miRNPs. The crosslinked sites are revealed by thymidine to cytidine transitions in the cDNAs prepared from immunopurified RNPs of 4-thiouridine-treated cells. We determined the binding sites and regulatory consequences for several intensely studied RBPs and miRNPs, including PUM2, QKI, IGF2BP1-3, AGO/EIF2C1-4 and TNRC6A-C. Our study revealed that these factors bind thousands of sites containing defined sequence motifs and have distinct preferences for exonic versus intronic or coding versus untranslated transcript regions. The precise mapping of binding sites across the transcriptome will be critical to the interpretation of the rapidly emerging data on genetic variation between individuals and how these variations contribute to complex genetic diseases.
LinkOut: [PMID: 20371350]
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Experimental Support 2 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | HEK293 |
Disease | 64859.0 |
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 GSM714642. RNA binding protein: AGO2. Condition:completeT1
... - Kishore S; Jaskiewicz L; Burger L; Hausser et al., 2011, Nature methods. |
Article |
- Kishore S; Jaskiewicz L; Burger L; Hausser et al. - Nature methods, 2011
Cross-linking and immunoprecipitation (CLIP) is increasingly used to map transcriptome-wide binding sites of RNA-binding proteins. We developed a method for CLIP data analysis, and applied it to compare CLIP with photoactivatable ribonucleoside-enhanced CLIP (PAR-CLIP) and to uncover how differences in cross-linking and ribonuclease digestion affect the identified sites. We found only small differences in accuracies of these methods in identifying binding sites of HuR, which binds low-complexity sequences, and Argonaute 2, which has a complex binding specificity. We found that cross-link-induced mutations led to single-nucleotide resolution for both PAR-CLIP and CLIP. Our results confirm the expectation from original CLIP publications that RNA-binding proteins do not protect their binding sites sufficiently under the denaturing conditions used during the CLIP procedure, and we show that extensive digestion with sequence-specific RNases strongly biases the recovered binding sites. This bias can be substantially reduced by milder nuclease digestion conditions.
LinkOut: [PMID: 21572407]
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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 |
Disease | 64859.0 |
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 GSM1065669. RNA binding protein: AGO1. Condition:4-thiouridine
... - Memczak S; Jens M; Elefsinioti A; Torti F; et al., 2013, Nature. |
Article |
- Memczak S; Jens M; Elefsinioti A; Torti F; et al. - Nature, 2013
Circular RNAs (circRNAs) in animals are an enigmatic class of RNA with unknown function. To explore circRNAs systematically, we sequenced and computationally analysed human, mouse and nematode RNA. We detected thousands of well-expressed, stable circRNAs, often showing tissue/developmental-stage-specific expression. Sequence analysis indicated important regulatory functions for circRNAs. We found that a human circRNA, antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as), is densely bound by microRNA (miRNA) effector complexes and harbours 63 conserved binding sites for the ancient miRNA miR-7. Further analyses indicated that CDR1as functions to bind miR-7 in neuronal tissues. Human CDR1as expression in zebrafish impaired midbrain development, similar to knocking down miR-7, suggesting that CDR1as is a miRNA antagonist with a miRNA-binding capacity ten times higher than any other known transcript. Together, our data provide evidence that circRNAs form a large class of post-transcriptional regulators. Numerous circRNAs form by head-to-tail splicing of exons, suggesting previously unrecognized regulatory potential of coding sequences.
LinkOut: [PMID: 23446348]
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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 | 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 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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CLIP-seq Support 1 for dataset GSM714642 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293 / completeT1, repA |
Location of target site | ENST00000410026.2 | 3UTR | CCCUACUUGAACACUUAUUGCACUUUUAUUUAUUGUU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 21572407 / GSE28865 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 for dataset GSM545212 | |
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Method / RBP | PAR-CLIP / AGO1 |
Cell line / Condition | HEK293 / Control |
Location of target site | ENST00000410026.2 | 3UTR | CCCUACUUGAACACUUAUUGCACUUUUAUUUAUUG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 20371350 / GSE21578 |
CLIP-seq Viewer | Link |
CLIP-seq Support 3 for dataset GSM545214 | |
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Method / RBP | PAR-CLIP / AGO3 |
Cell line / Condition | HEK293 / Control |
Location of target site | ENST00000410026.2 | 3UTR | CCCUACUUGAACACUUAUUGCACUUUUAU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 20371350 / GSE21578 |
CLIP-seq Viewer | Link |
CLIP-seq Support 4 for dataset GSM545217 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | HEK293 / miR-7 transfection |
Location of target site | ENST00000410026.2 | 3UTR | CCCUACUUGAACACUUAUUGCACUUUUAUUUA |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 20371350 / GSE21578 |
CLIP-seq Viewer | Link |
CLIP-seq Support 5 for dataset GSM1065669 | |
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Method / RBP | PAR-CLIP / AGO1 |
Cell line / Condition | HEK293 / 4-thiouridine, ML_MM_8 |
Location of target site | ENST00000410026.2 | 3UTR | CCCUACUUGAACACUUAUUGCACUUUUAUUUAUU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23446348 / GSE43573 |
CLIP-seq Viewer | Link |
MiRNA-Target Expression Profile | |||||||
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MiRNA-Target Expression Profile (TCGA) | |||||||
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65 hsa-miR-124-5p Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT064177 | KIAA1804 | mitogen-activated protein kinase kinase kinase 21 | 2 | 2 | ||||||||
MIRT069736 | FOXG1 | forkhead box G1 | 2 | 4 | ||||||||
MIRT086429 | NABP1 | nucleic acid binding protein 1 | 2 | 6 | ||||||||
MIRT105334 | SLC7A2 | solute carrier family 7 member 2 | 2 | 4 | ||||||||
MIRT110455 | PLEKHA1 | pleckstrin homology domain containing A1 | 2 | 2 | ||||||||
MIRT172998 | YTHDF3 | YTH N6-methyladenosine RNA binding protein 3 | 2 | 2 | ||||||||
MIRT196428 | TAOK1 | TAO kinase 1 | 2 | 14 | ||||||||
MIRT325704 | CSTF2 | cleavage stimulation factor subunit 2 | 2 | 2 | ||||||||
MIRT365670 | TSC22D3 | TSC22 domain family member 3 | 2 | 4 | ||||||||
MIRT365873 | XIAP | X-linked inhibitor of apoptosis | 2 | 2 | ||||||||
MIRT404126 | ASB1 | ankyrin repeat and SOCS box containing 1 | 2 | 2 | ||||||||
MIRT404626 | LCOR | ligand dependent nuclear receptor corepressor | 2 | 2 | ||||||||
MIRT405284 | ARF1 | ADP ribosylation factor 1 | 2 | 2 | ||||||||
MIRT406099 | PAGR1 | PAXIP1 associated glutamate rich protein 1 | 2 | 2 | ||||||||
MIRT446627 | SDC3 | syndecan 3 | 2 | 2 | ||||||||
MIRT446906 | RGS5 | regulator of G protein signaling 5 | 2 | 2 | ||||||||
MIRT461790 | FXR2 | FMR1 autosomal homolog 2 | 2 | 2 | ||||||||
MIRT463982 | WEE1 | WEE1 G2 checkpoint kinase | 2 | 4 | ||||||||
MIRT464204 | VGLL4 | vestigial like family member 4 | 2 | 2 | ||||||||
MIRT472790 | MTMR4 | myotubularin related protein 4 | 2 | 4 | ||||||||
MIRT473485 | MCFD2 | multiple coagulation factor deficiency 2 | 2 | 2 | ||||||||
MIRT481124 | AZIN1 | antizyme inhibitor 1 | 2 | 4 | ||||||||
MIRT485060 | SUCO | SUN domain containing ossification factor | 2 | 2 | ||||||||
MIRT487343 | HLA-DRA | major histocompatibility complex, class II, DR alpha | 2 | 2 | ||||||||
MIRT491948 | VPS52 | VPS52, GARP complex subunit | 2 | 2 | ||||||||
MIRT497208 | CDH7 | cadherin 7 | 2 | 2 | ||||||||
MIRT497476 | TOR1AIP2 | torsin 1A interacting protein 2 | 2 | 2 | ||||||||
MIRT528203 | NELFE | negative elongation factor complex member E | 2 | 2 | ||||||||
MIRT529255 | TRIM4 | tripartite motif containing 4 | 2 | 4 | ||||||||
MIRT530096 | PSAPL1 | prosaposin like 1 (gene/pseudogene) | 2 | 2 | ||||||||
MIRT530597 | C7orf33 | chromosome 7 open reading frame 33 | 2 | 4 | ||||||||
MIRT534980 | PSAT1 | phosphoserine aminotransferase 1 | 2 | 4 | ||||||||
MIRT538326 | CSGALNACT1 | chondroitin sulfate N-acetylgalactosaminyltransferase 1 | 2 | 2 | ||||||||
MIRT561237 | ZNF652 | zinc finger protein 652 | 2 | 2 | ||||||||
MIRT562035 | KRAS | KRAS proto-oncogene, GTPase | 2 | 2 | ||||||||
MIRT563120 | THAP5 | THAP domain containing 5 | 2 | 2 | ||||||||
MIRT563538 | RBM41 | RNA binding motif protein 41 | 2 | 2 | ||||||||
MIRT566037 | REV3L | REV3 like, DNA directed polymerase zeta catalytic subunit | 2 | 2 | ||||||||
MIRT566505 | PAWR | pro-apoptotic WT1 regulator | 2 | 2 | ||||||||
MIRT566745 | MRPL35 | mitochondrial ribosomal protein L35 | 2 | 2 | ||||||||
MIRT566850 | LRRC58 | leucine rich repeat containing 58 | 2 | 2 | ||||||||
MIRT568077 | CELF2 | CUGBP Elav-like family member 2 | 2 | 2 | ||||||||
MIRT576826 | Tgfbr3 | transforming growth factor, beta receptor III | 2 | 2 | ||||||||
MIRT608870 | NR2E1 | nuclear receptor subfamily 2 group E member 1 | 2 | 4 | ||||||||
MIRT611997 | VAC14 | Vac14, PIKFYVE complex component | 2 | 2 | ||||||||
MIRT614054 | FAM89A | family with sequence similarity 89 member A | 2 | 2 | ||||||||
MIRT618800 | SPATA21 | spermatogenesis associated 21 | 2 | 2 | ||||||||
MIRT619389 | RSPH3 | radial spoke head 3 homolog | 2 | 2 | ||||||||
MIRT622282 | SH3TC2 | SH3 domain and tetratricopeptide repeats 2 | 2 | 2 | ||||||||
MIRT624026 | EN2 | engrailed homeobox 2 | 2 | 2 | ||||||||
MIRT626000 | MPEG1 | macrophage expressed 1 | 2 | 2 | ||||||||
MIRT641792 | USP32 | ubiquitin specific peptidase 32 | 2 | 2 | ||||||||
MIRT651599 | WDFY2 | WD repeat and FYVE domain containing 2 | 2 | 2 | ||||||||
MIRT659662 | CDC73 | cell division cycle 73 | 2 | 2 | ||||||||
MIRT663010 | KIAA1586 | KIAA1586 | 2 | 2 | ||||||||
MIRT663561 | ASTN2 | astrotactin 2 | 2 | 2 | ||||||||
MIRT669312 | C16orf72 | chromosome 16 open reading frame 72 | 2 | 2 | ||||||||
MIRT685216 | POTED | POTE ankyrin domain family member D | 2 | 2 | ||||||||
MIRT695757 | ZNF117 | zinc finger protein 117 | 2 | 2 | ||||||||
MIRT697909 | TXNRD1 | thioredoxin reductase 1 | 2 | 2 | ||||||||
MIRT707181 | RPH3A | rabphilin 3A | 2 | 2 | ||||||||
MIRT707214 | TRIM13 | tripartite motif containing 13 | 2 | 2 | ||||||||
MIRT707478 | SLCO4C1 | solute carrier organic anion transporter family member 4C1 | 2 | 2 | ||||||||
MIRT719507 | LMAN2L | lectin, mannose binding 2 like | 2 | 2 | ||||||||
MIRT755814 | PARP1 | poly(ADP-ribose) polymerase 1 | 2 | 1 |
miRNA-Drug Associations | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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miRNA-Drug Resistance Associations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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