pre-miRNA Information | |
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pre-miRNA | mmu-mir-122 |
Genomic Coordinates | chr18: 65248861 - 65248926 |
Synonyms | Mirn122a, mmu-mir-122, Mir122a |
Description | Mus musculus miR-122 stem-loop |
Comment | The mature sequence shown here represents the most commonly cloned form from large-scale cloning studies . |
RNA Secondary Structure |
Mature miRNA Information | |
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Mature miRNA | mmu-miR-122-5p |
Sequence | 6| UGGAGUGUGACAAUGGUGUUUG |27 |
Evidence | Experimental |
Experiments | Cloned |
Putative Targets |
Biomarker Information |
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Gene Information | |||||||||||||||||||||
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Gene Symbol | Slc7a1 | ||||||||||||||||||||
Synonyms | 4831426K01Rik, AI447493, Atrc-1, Atrc1, Cat1, Rec-1, Rev-1, mCAT-1 | ||||||||||||||||||||
Description | solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 | ||||||||||||||||||||
Transcript | NM_007513 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on Slc7a1 | |||||||||||||||||||||
3'UTR of Slc7a1 (miRNA target sites are highlighted) |
>Slc7a1|NM_007513|3'UTR 1 CGTGCAGCCCCACCCACCAGGGTGACAGCGGTTGACGGGTGCCCGTAGAAGCCTGGGACCCTCACAATCTCTCCACTCAT 81 GCCTCAGGATCAGCTCACACCCCCAATGTCACCAAAGCTGGTTTGCTGCCAGCTCGTGAGATCCTGGTCATTTCTGGACA 161 GTCCCTTGGTTTACTCATCTCCCTCTGAACAAAGAAAGCAGCCCTTCTCCTTGCCGGCCGGCCGGGCGCTTCGCTGCTGC 241 GGCCCCAGCAGAAGGGAGGCCCCCTTCTCCTCTCACTTGGGAAGCAGGCCTCCCTCCCTCCCTGGGACCACCCTGGCATC 321 GCCCATGTGCACACTCCAGATGGCTAGTGAGCCTCTCCCTGTCAGCCCAGGACAGTCTCCTGACCACAAGATGCAAGACT 401 ATCCCAGCGAGGAAGCATGTGCCCCAACAGTGCTGCCCGACAGCCCATCAACTACAGAATACCTAAAGAGGAGGAACAGG 481 CCCACATCTTACTGCTTTCTGGCTGGGGTGGTAGGATGGGGTCCCGGGTCTGCACAGAAGCATCTGTGCAGAACACAGCA 561 CGGTGTGAGCCGTTCAGGTGTGAGCCGCTCATCTCGAGCACAGAAGACGGGAGATCCCTGGAGTGACCAGTAGTGTCGAG 641 ATGAGACGGCCAGCTCAGCCCGCGTGGACTAGGGTGACATTCTCTGGTCTCATTCCTAGCAGGCCTGGGTTGGCTTTTGC 721 TGCTCTTGGCGCCTTGTCCCCACTGTCCTGAGTCACTGGAACACAAGGCTGTATCCGTAGGGTTATTTCATTCTCTCGGG 801 TCTTCTAAAGTTCTTCAGACAGGTGGCACTCAATGTGGGGTGGTGACGCCTTTCTGGCCACTGACGTGATCTGTGTGGCC 881 TTTTACATCTAAGGAGTACTGCGGAGTCCTCCCCCTGCTGCTTGCTGTGAATCACTCCACTGGATTAACTTGGGGCTTAA 961 TGTTACCTTGGAAGATAGCCAAATCATTACCGACTGCCATATCAGCTTGCGGTTCAAGATGTGTGGCCTGCGCAGGAGAT 1041 GGCTTGGGGTCCTATTGCTATTCCTCTTGTAGCTGTGGTGCCTTTGCCTGCTGCTGGTGAGATTTCCACCCTGGCCTGGA 1121 CCTTATTCCCCTTCATTTCCCCTCCCCCACCCCACGCTCCATATCTCTCGGGGTGTGGCCTGAGGGCTGACACCTCTTCA 1201 TTTACTCTTTGTAGATAGAAACTGCTTGAGAGTGCTGGTGGATTCTCAGAACCAGCAGGGTGCCCTTCCCCCACCCCACA 1281 TCCCCCTTCCACCATATTGGGGTGGCGAAGCCTAGTGTCTTAGTCTAATGTTAATGCTGTTTATAAAGCCAAGCTTTCTT 1361 TTCTGTCTGGCTTTTGACCCAAGTCTGGTGGAAACAGGCTGAGTAGGTAGACTGATGGCCCTGTCTTTCCTCTGCTTTGG 1441 AAGATTCTTGAGAATGGAAGAGTTAGTGGGGCTGGACAGGCGTGTAGCCTAGTGGTAGCACACTTCCCCAGCCTACACAG 1521 GGCCTCAGCTTCCACCCCCAGCACTACGTATGGAAAATTAGGGAGATTAGAGAAACCACCTAATTGCTGGGTCAGCCAGT 1601 GGAGGACAGCTGAGCATCCAAGAGCCAGGCCCTGACCACCGTCCAGGCACTTTGTCTCCTAGGCTGCCTGAAAACACTGC 1681 AAAGGGAGTATTATAAGACCCTACATGTTGAGTTTCTAAAGGTATTTAAAGTTATGTAGATTGGTGCTGTAAAATATTTT 1761 GATAAATATTAACTTATTTTATTCGGGTCTTGATTACCTATTGTCTTCTTAGGGTCTGTTAAGTATCTGTCTGGGTTTTT 1841 TTTTTCCTTGTTACTTGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGCCCAGTGAGGTGTTGGAAG 1921 AATCTTTTAAAGTTTAGTGTCTTTGGCTTCTTTTTTGAGACAAGGTTTCACACTCTAGCTGGCCTGGAATAGGATTATCG 2001 TTGCCCAGTGTGGCCTCTGCCTCAGGCTCCCGAGTGCTAAGAGCATAGGCGTGAGCCTCCGCTCCTCCTGCTGAACTGTC 2081 TCTTGCTTTCTGGGTAAAACCTCCCTGTCTAAGGCAGCCTAACCATGTGTTTACAGTTGACGTTTCAGCCAGCAGCTTGT 2161 ATCCCACCAAGGGGAAAGGTGTGTATCTAGGGGTTTGATCTGTCACCATCCCTCCTGAGGACCGCAAGCAACGGTCTATA 2241 TATACATCTGTTCTATATGTTTCCCTGTGCGACACAGGAGCAAACACAGGCCCTGGCGGGGTGGGGTGGGGTCGGGGGGG 2321 GGGGCATCCTGAACCCACTTCCTAGTCAGGAAAAGATGCTTGAAGGCGGTGTGCCTAGTTAGTTGATTGGCCACTGAGCT 2401 CTTACTAAGAGTGGACACTTTTGGGGGTACACAGGAACAATGATGTATATAGTTATGCCTGGAGCGAGCCTCTAATGTGC 2481 TTTTTATTATGCCCCCAGTTCCTTCTGAAAGGAAAACACAAGCCCCAAACCCAAACAACACACACACACACACACACACA 2561 CACACACACACACACACACACACACACACACATCCCTCCAGACCAACAGCAGGTGGTATCCCGTCTCCTAGCCTCCTGCC 2641 CAAAGAAGAGTCCCATTGGGTTTCAAAGCATGGCCAGCATTTCCTACCTAGCTGGAACTTAGACATTCTAAAGACACATT 2721 CCCATGCCTTGTTTACCTGCAGCTAGTATATTCACATTGAAAAGACCCATTTTTCCAGGAGCCTGTGCTCTTCCTGTCTC 2801 TGGGTCTAAGTTCATGAAGAAGCCAATACCCAGGAGTGGGGCACAAGATGTCTCCACCTTTCAGAAGGTGGCCCTGGTCA 2881 TGGTGGTAGTGGTAGGTGGTGTCTATAGAGACATTAACCCTCCCACCCCACACCCCCGTGTATATTTGTGGAAGGGTGGG 2961 TGCACACCTAGGCCCATCCCCCATCCCTGCCCATCTCCTACAGCCAGGCCTTTGTGGATTTATTTTGCAAACAAAGAAAA 3041 AATGAGAGTCTGACCCGGGCAGTTTCTGGAAGATTGCTGGCTTTATTCTGTTTTCAGTTGTTCACAGTTTGGTTTTACAG 3121 TATGCAAATTCTGCCTGTCATCTGATATCCCCTCTGCTGGTGACTTGACTTGGGAACCACATACCAAGCACCTGCCTGAG 3201 GCTTGATGGTCAGAAGTGTCTGCAGGTTTCTCCACCTGCCCCTAGCAGCCAAGGGTTGGACATACCCCACCCCCAGCCCC 3281 AACTCCTGAGCACATCTGGTACAGCCGGTGTGTGCACAGCTAAGGGAATATGTACCCTGCTCCACCTGTCTACTGCCTGA 3361 TGCTCTCATGCATAGGGCTGGGATTACCAGTGGCCGTGTTTGTACCTTGGCCCTAACCCCACACAGACATTCTGAATTTC 3441 GGAGTGTTCATAGTCTCCTCTAGCAAGGAACTTGCCCAGCACTGGGTAGAAGCTTGGCAACAGCAGTGTGAGAGACCGGG 3521 TTCCTAGGATAAGCGTGGACACGCCCCACGGGCTCACTCATGTCTACTGGCAAAGCCATGGCCACTGCTGATCTGTGTAC 3601 CTCCCTGCAATGGAAACATGGCTGGCTTCCGCCAGGGCCCATCCTTTCTGACTTGAGCATCTTATGTCCCCACAGATAGT 3681 TATTTCATCCTAATAAAAGCTTACTGTTTTGTTGGCTCCCAAGCATTAAGGAATCTTAAGTGGGGAATCTAAGTGCCAGG 3761 GTGCCCACCCCTTGGGGTGTTGGTGGGTGATGCAAACAGGGATGTTTGAGTCCAGGTATGGTTGGGCTAGCGAAGGGAGT 3841 GGCCAGACAGAGAATACATGGCCCATGGAACTGTTAGAGAACTCAGAGTCAGCGCTGAATGTATGTCATGTTATATAATT 3921 CAAACCGCGTCTGTTTGCCTTCATCATGAGAGGATTGTACATAAGGTTCCTGGGGGGAGAGCGAGTGGTCCGTTTCTTTA 4001 GGCTTGTTTTGGTTTGCGAAATACTTTGATTGTCACAGTGGTGCAAGTGAAACGTGCTACACTCCAATGTGGTTAGGATG 4081 AAAATTTTAGGGCAAAAATAAATAAATAAAAATTAAAAAAAAAATCTACCAGCTGGTTTTCACCTCCGTTACGCTCGCCT 4161 GGTCTTTCTGTGTCCACTGCTCCACTGAGCCGGGGAATATGGTGTAGCCAAAGGTCTTGAGACACGGTGATGACCAAGGA 4241 GCCTTCCTGGACCATCCTGTTACACGTGCTGAATGGCTGGCTCAAAAGCCCAGGAGAGACGAAAGTCCATGTCCAAAGAT 4321 GTTCTCAGGGCGCTGGCACGTCCAGCAGTGTCAGGAAGCAAGGTTTAGGAAGCTACATCATGCACGCTAGTTTATTGATA 4401 AGTGTCACCTTTCGTGCTCTGACAAGCTTTTTGAGTTTGGAACTTATTTTCCAATTTGAGAAGTTATAATATATCTTTGT 4481 ATTTAAGATATTTACTGCTTTGTTTGTGCCTTGAAGCTTCGATGGGTTTAAGGATCACAGAGGGGCCAGGATACTAACGA 4561 GGGCTGGTTTATTTGCAAACCTGAATACTTGTGTTGTGGTTTCTCCAGGACAATTTTTTTATTATTATTTCTACTGAACA 4641 TGGAGCCATTATTAAAAAGAGTTATGTGTGGTTTTTCATTATGTAAATTGTATATATATTTTTTTGCTTGTTTGAGGTTC 4721 TATTTTTCTAATAGTCTTCTTACAGTTTCTTATAATGATGACATTAGATTAAGTCCGATACTAACTGTAAATCAAGCTGG 4801 TTTCTGCTGGATTCCCGTGGATTAATTCTATTTTATTTTAAGGCCAAGTGCAGGTGTCATCCACCACCCTTTTGAAAAAA 4881 AATGTGAAATTTATGTTTCCCCTCGTTGCTGAATACATTGTACACTGGCAAGACCCCTCCCATACTTATGTGTTGTAAAA 4961 TCAAAGCTGTTTTGTGGTACATTGTGTCATGCTCCTGCAGACGCTAATAAACCCTGTCTGGCTTCCACAAAAAAAAAAAA 5041 AAAAAA 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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Experimental Support 1 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Location of target site | 3'UTR |
Article |
- Esau C; Davis S; Murray SF; Yu XX; Pandey et al. - Cell metabolism, 2006
Current understanding of microRNA (miRNA) biology is limited, and antisense oligonucleotide (ASO) inhibition of miRNAs is a powerful technique for their functionalization. To uncover the role of the liver-specific miR-122 in the adult liver, we inhibited it in mice with a 2'-O-methoxyethyl phosphorothioate ASO. miR-122 inhibition in normal mice resulted in reduced plasma cholesterol levels, increased hepatic fatty-acid oxidation, and a decrease in hepatic fatty-acid and cholesterol synthesis rates. Activation of the central metabolic sensor AMPK was also increased. miR-122 inhibition in a diet-induced obesity mouse model resulted in decreased plasma cholesterol levels and a significant improvement in liver steatosis, accompanied by reductions in several lipogenic genes. These results implicate miR-122 as a key regulator of cholesterol and fatty-acid metabolism in the adult liver and suggest that miR-122 may be an attractive therapeutic target for metabolic disease.
LinkOut: [PMID: 16459310]
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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 | Huh7 , HepG2 , 293T , AML-12 , WC-3 |
Location of target site | 3'UTR |
Article |
- Chang J; Nicolas E; Marks D; Sander C; et al. - RNA biology, 2004
These studies show that miR-122, a 22-nucleotide microRNA, is derived from a liver-specific noncoding polyadenylated RNA transcribed from the gene hcr. The exact sequence of miR-122 as well as the adjacent secondary structure within the hcr mRNA are conserved from mammalian species back to fish. Levels of miR-122 in the mouse liver increase to half maximal values around day 17 of embryogenesis, and reach near maximal levels of 50,000 copies per average cell before birth. Lewis et al. (2003) predicted the cationic amino acid transporter (CAT-1 or SLC7A1) as a miR-122 target. CAT-1 protein and its mRNA are expressed in all mammalian tissues but with lower levels in adult liver. Furthermore, during mouse liver development CAT-1 mRNA decreases in an almost inverse correlation with miR-122. Eight potential miR-122 target sites were predicted within the human CAT-1 mRNA, with six in the 3'-untranslated region. Using a reporter construct it was found that just three of the predicted sites, linked in a 400-nucleotide sequence from human CAT-1, acted with synergy and were sufficient to strongly inhibit protein synthesis and reduce mRNA levels. In summary, these studies followed the accumulation during development of miR-122 from its mRNA precursor, hcr, through to identification of what may be a specific mRNA target, CAT-1.
LinkOut: [PMID: 17179747]
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Experimental Support 3 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Article |
- Gatfield D; Le Martelot G; Vejnar CE; et al. - Genes & development, 2009
In liver, most metabolic pathways are under circadian control, and hundreds of protein-encoding genes are thus transcribed in a cyclic fashion. Here we show that rhythmic transcription extends to the locus specifying miR-122, a highly abundant, hepatocyte-specific microRNA. Genetic loss-of-function and gain-of-function experiments have identified the orphan nuclear receptor REV-ERBalpha as the major circadian regulator of mir-122 transcription. Although due to its long half-life mature miR-122 accumulates at nearly constant rates throughout the day, this miRNA is tightly associated with control mechanisms governing circadian gene expression. Thus, the knockdown of miR-122 expression via an antisense oligonucleotide (ASO) strategy resulted in the up- and down-regulation of hundreds of mRNAs, of which a disproportionately high fraction accumulates in a circadian fashion. miR-122 has previously been linked to the regulation of cholesterol and lipid metabolism. The transcripts associated with these pathways indeed show the strongest time point-specific changes upon miR-122 depletion. The identification of Pparbeta/delta and the peroxisome proliferator-activated receptor alpha (PPARalpha) coactivator Smarcd1/Baf60a as novel miR-122 targets suggests an involvement of the circadian metabolic regulators of the PPAR family in miR-122-mediated metabolic control.
LinkOut: [PMID: 19487572]
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86 mmu-miR-122-5p Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT003075 | Tmem50b | transmembrane protein 50B | 1 | 1 | ||||||||
MIRT003076 | Lass6 | ceramide synthase 6 | 1 | 1 | ||||||||
MIRT003077 | Gpx7 | glutathione peroxidase 7 | 1 | 1 | ||||||||
MIRT003113 | Tgfbr1 | transforming growth factor, beta receptor I | 3 | 1 | ||||||||
MIRT003114 | Sbk1 | SH3-binding kinase 1 | 3 | 1 | ||||||||
MIRT003117 | Hist1h1c | histone cluster 1, H1c | 3 | 1 | ||||||||
MIRT003118 | Ddc | dopa decarboxylase | 2 | 1 | ||||||||
MIRT003120 | Rell1 | RELT-like 1 | 3 | 1 | ||||||||
MIRT003121 | Bach1 | BTB and CNC homology 1, basic leucine zipper transcription factor 1 | 2 | 1 | ||||||||
MIRT003122 | Apob | apolipoprotein B | 2 | 1 | ||||||||
MIRT003123 | P4ha1 | procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha 1 polypeptide | 2 | 1 | ||||||||
MIRT003124 | Ccng1 | cyclin G1 | 2 | 1 | ||||||||
MIRT003125 | Slc7a1 | solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 | 3 | 3 | ||||||||
MIRT003126 | Gys1 | glycogen synthase 1, muscle | 2 | 2 | ||||||||
MIRT003127 | Slc35a4 | solute carrier family 35, member A4 | 2 | 2 | ||||||||
MIRT003128 | Hfe2 | hemochromatosis type 2 (juvenile) | 3 | 3 | ||||||||
MIRT003129 | Tmed3 | transmembrane p24 trafficking protein 3 | 2 | 2 | ||||||||
MIRT003132 | Bckdk | branched chain ketoacid dehydrogenase kinase | 4 | 1 | ||||||||
MIRT003133 | Aldoa | aldolase A, fructose-bisphosphate | 4 | 7 | ||||||||
MIRT003134 | Ndrg3 | N-myc downstream regulated gene 3 | 4 | 2 | ||||||||
MIRT003135 | Cd320 | CD320 antigen | 4 | 1 | ||||||||
MIRT003724 | Smarcd1 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 | 3 | 1 | ||||||||
MIRT003725 | Rcan1 | regulator of calcineurin 1 | 2 | 1 | ||||||||
MIRT003726 | Gde1 | glycerophosphodiester phosphodiesterase 1 | 2 | 1 | ||||||||
MIRT004536 | Ccrn4l | nocturnin | 4 | 1 | ||||||||
MIRT005975 | Klf6 | Kruppel-like factor 6 | 4 | 1 | ||||||||
MIRT005976 | B2m | beta-2 microglobulin | 1 | 1 | ||||||||
MIRT005977 | Afp | alpha fetoprotein | 1 | 1 | ||||||||
MIRT005978 | Ccl2 | chemokine (C-C motif) ligand 2 | 1 | 1 | ||||||||
MIRT005979 | Csf3r | colony stimulating factor 3 receptor (granulocyte) | 1 | 1 | ||||||||
MIRT005980 | Ctgf | connective tissue growth factor | 1 | 1 | ||||||||
MIRT005981 | Cxcl13 | chemokine (C-X-C motif) ligand 13 | 1 | 1 | ||||||||
MIRT005982 | Cyp2b13 | cytochrome P450, family 2, subfamily b, polypeptide 13 | 1 | 1 | ||||||||
MIRT005983 | Dbp | D site albumin promoter binding protein | 1 | 1 | ||||||||
MIRT005984 | Igf2 | insulin-like growth factor 2 | 1 | 1 | ||||||||
MIRT005985 | Il1b | interleukin 1 beta | 1 | 1 | ||||||||
MIRT005986 | Jun | jun proto-oncogene | 1 | 1 | ||||||||
MIRT005987 | Per1 | period circadian clock 1 | 1 | 1 | ||||||||
MIRT005988 | Alpl | alkaline phosphatase, liver/bone/kidney | 2 | 1 | ||||||||
MIRT005989 | Cs | citrate synthase | 2 | 1 | ||||||||
MIRT005990 | Prom1 | prominin 1 | 3 | 1 | ||||||||
MIRT005991 | Sox4 | SRY (sex determining region Y)-box 4 | 3 | 1 | ||||||||
MIRT013527 | Uros | uroporphyrinogen III synthase | 1 | 1 | ||||||||
MIRT013528 | Ppox | protoporphyrinogen oxidase | 1 | 1 | ||||||||
MIRT013529 | Urod | uroporphyrinogen decarboxylase | 1 | 1 | ||||||||
MIRT013530 | Cpox | coproporphyrinogen oxidase | 1 | 1 | ||||||||
MIRT013531 | Fech | ferrochelatase | 1 | 1 | ||||||||
MIRT013532 | Hamp | hepcidin antimicrobial peptide | 1 | 1 | ||||||||
MIRT013533 | Tfr2 | transferrin receptor 2 | 1 | 1 | ||||||||
MIRT013534 | Smad4 | SMAD family member 4 | 1 | 1 | ||||||||
MIRT013535 | Smad7 | SMAD family member 7 | 1 | 1 | ||||||||
MIRT013536 | Bmpr1a | bone morphogenetic protein receptor, type 1A | 1 | 1 | ||||||||
MIRT013537 | Hba-a1 | hemoglobin alpha, adult chain 1 | 2 | 1 | ||||||||
MIRT013538 | Hmbs | hydroxymethylbilane synthase | 2 | 1 | ||||||||
MIRT013539 | Mir17 | microRNA 17 | 2 | 1 | ||||||||
MIRT013540 | Alas2 | aminolevulinic acid synthase 2, erythroid | 2 | 1 | ||||||||
MIRT013541 | Mir451 | microRNA 451a | 2 | 1 | ||||||||
MIRT013542 | Tfrc | transferrin receptor | 2 | 1 | ||||||||
MIRT013543 | Socs2 | suppressor of cytokine signaling 2 | 1 | 1 | ||||||||
MIRT013544 | Slc35g1 | solute carrier family 35, member G1 | 1 | 1 | ||||||||
MIRT013545 | Camk2b | calcium/calmodulin-dependent protein kinase II, beta | 1 | 1 | ||||||||
MIRT013546 | Irf6 | interferon regulatory factor 6 | 1 | 1 | ||||||||
MIRT013547 | Rbl2 | RB transcriptional corepressor like 2 | 1 | 1 | ||||||||
MIRT013548 | Hfe | hemochromatosis | 2 | 1 | ||||||||
MIRT013549 | Ccnd1 | cyclin D1 | 2 | 1 | ||||||||
MIRT054338 | Pkm | pyruvate kinase, muscle | 3 | 1 | ||||||||
MIRT054339 | Tfdp2 | transcription factor Dp 2 | 3 | 1 | ||||||||
MIRT054340 | E2f1 | E2F transcription factor 1 | 3 | 1 | ||||||||
MIRT579817 | Zfp113 | zinc finger protein 113 | 1 | 1 | ||||||||
MIRT580378 | Tmem206 | transmembrane protein 206 | 1 | 2 | ||||||||
MIRT581166 | Sec23ip | Sec23 interacting protein | 1 | 1 | ||||||||
MIRT582514 | March5 | membrane-associated ring finger (C3HC4) 5 | 1 | 2 | ||||||||
MIRT586941 | H2-T24 | histocompatibility 2, T region locus 24 | 1 | 2 | ||||||||
MIRT591859 | Iffo2 | intermediate filament family orphan 2 | 1 | 1 | ||||||||
MIRT592160 | Paxip1 | PAX interacting (with transcription-activation domain) protein 1 | 1 | 1 | ||||||||
MIRT592189 | Nanog | Nanog homeobox | 1 | 2 | ||||||||
MIRT592792 | Cdh12 | cadherin 12 | 1 | 1 | ||||||||
MIRT597026 | Thap1 | THAP domain containing, apoptosis associated protein 1 | 1 | 1 | ||||||||
MIRT597210 | Snhg11 | small nucleolar RNA host gene 11 | 1 | 1 | ||||||||
MIRT601300 | Zfp949 | zinc finger protein 949 | 1 | 1 | ||||||||
MIRT602608 | Chrna1 | cholinergic receptor, nicotinic, alpha polypeptide 1 (muscle) | 1 | 1 | ||||||||
MIRT602960 | Xpo7 | exportin 7 | 1 | 1 | ||||||||
MIRT603391 | Sgol2 | shugoshin 2A | 1 | 1 | ||||||||
MIRT604008 | Ggps1 | geranylgeranyl diphosphate synthase 1 | 1 | 1 | ||||||||
MIRT605553 | Ppp1r16b | protein phosphatase 1, regulatory (inhibitor) subunit 16B | 1 | 1 | ||||||||
MIRT606204 | Sfxn4 | sideroflexin 4 | 1 | 1 |
miRNA-Drug Associations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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miRNA-Drug Resistance Associations | ||||||||||||||||||||||||||||||||||||||||
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