pre-miRNA Information | |
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pre-miRNA | hsa-mir-6752 |
Genomic Coordinates | chr11: 67490245 - 67490315 |
Description | Homo sapiens miR-6752 stem-loop |
Comment | None |
RNA Secondary Structure |
Mature miRNA Information | ||||||||||||||||
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Mature miRNA | hsa-miR-6752-3p | |||||||||||||||
Sequence | 51| UCCCUGCCCCCAUACUCCCAG |71 | |||||||||||||||
Evidence | Experimental | |||||||||||||||
Experiments | Meta-analysis | |||||||||||||||
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 | CDKN1A | ||||||||||||||||||||
Synonyms | CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | ||||||||||||||||||||
Description | cyclin dependent kinase inhibitor 1A | ||||||||||||||||||||
Transcript | NM_000389 | ||||||||||||||||||||
Other Transcripts | NM_078467 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on CDKN1A | |||||||||||||||||||||
3'UTR of CDKN1A (miRNA target sites are highlighted) |
>CDKN1A|NM_000389|3'UTR 1 TCCGCCCACAGGAAGCCTGCAGTCCTGGAAGCGCGAGGGCCTCAAAGGCCCGCTCTACATCTTCTGCCTTAGTCTCAGTT 81 TGTGTGTCTTAATTATTATTTGTGTTTTAATTTAAACACCTCCTCATGTACATACCCTGGCCGCCCCCTGCCCCCCAGCC 161 TCTGGCATTAGAATTATTTAAACAAAAACTAGGCGGTTGAATGAGAGGTTCCTAAGAGTGCTGGGCATTTTTATTTTATG 241 AAATACTATTTAAAGCCTCCTCATCCCGTGTTCTCCTTTTCCTCTCTCCCGGAGGTTGGGTGGGCCGGCTTCATGCCAGC 321 TACTTCCTCCTCCCCACTTGTCCGCTGGGTGGTACCCTCTGGAGGGGTGTGGCTCCTTCCCATCGCTGTCACAGGCGGTT 401 ATGAAATTCACCCCCTTTCCTGGACACTCAGACCTGAATTCTTTTTCATTTGAGAAGTAAACAGATGGCACTTTGAAGGG 481 GCCTCACCGAGTGGGGGCATCATCAAAAACTTTGGAGTCCCCTCACCTCCTCTAAGGTTGGGCAGGGTGACCCTGAAGTG 561 AGCACAGCCTAGGGCTGAGCTGGGGACCTGGTACCCTCCTGGCTCTTGATACCCCCCTCTGTCTTGTGAAGGCAGGGGGA 641 AGGTGGGGTCCTGGAGCAGACCACCCCGCCTGCCCTCATGGCCCCTCTGACCTGCACTGGGGAGCCCGTCTCAGTGTTGA 721 GCCTTTTCCCTCTTTGGCTCCCCTGTACCTTTTGAGGAGCCCCAGCTACCCTTCTTCTCCAGCTGGGCTCTGCAATTCCC 801 CTCTGCTGCTGTCCCTCCCCCTTGTCCTTTCCCTTCAGTACCCTCTCAGCTCCAGGTGGCTCTGAGGTGCCTGTCCCACC 881 CCCACCCCCAGCTCAATGGACTGGAAGGGGAAGGGACACACAAGAAGAAGGGCACCCTAGTTCTACCTCAGGCAGCTCAA 961 GCAGCGACCGCCCCCTCCTCTAGCTGTGGGGGTGAGGGTCCCATGTGGTGGCACAGGCCCCCTTGAGTGGGGTTATCTCT 1041 GTGTTAGGGGTATATGATGGGGGAGTAGATCTTTCTAGGAGGGAGACACTGGCCCCTCAAATCGTCCAGCGACCTTCCTC 1121 ATCCACCCCATCCCTCCCCAGTTCATTGCACTTTGATTAGCAGCGGAACAAGGAGTCAGACATTTTAAGATGGTGGCAGT 1201 AGAGGCTATGGACAGGGCATGCCACGTGGGCTCATATGGGGCTGGGAGTAGTTGTCTTTCCTGGCACTAACGTTGAGCCC 1281 CTGGAGGCACTGAAGTGCTTAGTGTACTTGGAGTATTGGGGTCTGACCCCAAACACCTTCCAGCTCCTGTAACATACTGG 1361 CCTGGACTGTTTTCTCTCGGCTCCCCATGTGTCCTGGTTCCCGTTTCTCCACCTAGACTGTAAACCTCTCGAGGGCAGGG 1441 ACCACACCCTGTACTGTTCTGTGTCTTTCACAGCTCCTCCCACAATGCTGAATATACAGCAGGTGCTCAATAAATGATTC 1521 TTAGTGACTTTACTTGTAAAAAAAAAAAAAAAAAA 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 | hESCs (WA-09) | ||||||
Disease | 1026.0 | ||||||
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 |
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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 | 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 ERX177603. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_2_5
PAR-CLIP data was present in ERX177628. RNA binding protein: AGO2. Condition:p53_V_AGO_CLIP_4_6
PAR-CLIP data was present in ERX177616. RNA binding protein: AGO2. Condition:p53_V_AGO_CLIP_3_6
PAR-CLIP data was present in ERX177627. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_4_5
PAR-CLIP data was present in ERX177631. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_4_9
PAR-CLIP data was present in ERX177619. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_3_9
PAR-CLIP data was present in ERX177615. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_3_5
... - 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 SRR359787 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | hESCs (WA-09) / 4-thiouridine, RNase T1 |
Location of target site | ENST00000244741.5 | 3UTR | AGGGCAGGGACCACACCCUGUACUGUUCUGUGUCUU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 22012620 / SRX103431 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 for dataset GSM1462572 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | C8166 / C8166 NL4-3 |
Location of target site | ENST00000244741.5 | 3UTR | ACCACACCCUGUACUGUUCUG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23592263 / GSE59944 |
CLIP-seq Viewer | Link |
CLIP-seq Support 3 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 | ENST00000244741.5 | 3UTR | UUUCUCCACCUAGACUGUAAACCUCUCGAGG |
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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110 hsa-miR-6752-3p Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT152341 | TNFSF9 | TNF superfamily member 9 | 2 | 2 | ||||||||
MIRT273594 | SP1 | Sp1 transcription factor | 2 | 2 | ||||||||
MIRT291927 | TPM4 | tropomyosin 4 | 2 | 4 | ||||||||
MIRT311186 | ANKRD33B | ankyrin repeat domain 33B | 2 | 4 | ||||||||
MIRT378521 | CDKN1A | cyclin dependent kinase inhibitor 1A | 2 | 4 | ||||||||
MIRT452467 | SORCS2 | sortilin related VPS10 domain containing receptor 2 | 2 | 2 | ||||||||
MIRT478636 | CTDNEP1 | CTD nuclear envelope phosphatase 1 | 2 | 2 | ||||||||
MIRT496343 | TMEM81 | transmembrane protein 81 | 2 | 2 | ||||||||
MIRT496646 | MFAP3 | microfibril associated protein 3 | 2 | 2 | ||||||||
MIRT496711 | DNAJC30 | DnaJ heat shock protein family (Hsp40) member C30 | 2 | 2 | ||||||||
MIRT499242 | VAV3 | vav guanine nucleotide exchange factor 3 | 2 | 4 | ||||||||
MIRT519777 | ZNF354B | zinc finger protein 354B | 2 | 6 | ||||||||
MIRT520883 | STX17 | syntaxin 17 | 2 | 2 | ||||||||
MIRT522476 | ZAK | mitogen-activated protein kinase kinase kinase 20 | 2 | 2 | ||||||||
MIRT523587 | G3BP2 | G3BP stress granule assembly factor 2 | 2 | 6 | ||||||||
MIRT525240 | KCNJ12 | potassium voltage-gated channel subfamily J member 12 | 2 | 2 | ||||||||
MIRT527025 | PABPN1L | poly(A) binding protein nuclear 1 like, cytoplasmic | 2 | 2 | ||||||||
MIRT527709 | IL17REL | interleukin 17 receptor E like | 2 | 2 | ||||||||
MIRT530778 | GPD1 | glycerol-3-phosphate dehydrogenase 1 | 2 | 2 | ||||||||
MIRT531883 | SCN1B | sodium voltage-gated channel beta subunit 1 | 2 | 2 | ||||||||
MIRT533043 | ZBTB46 | zinc finger and BTB domain containing 46 | 2 | 2 | ||||||||
MIRT535062 | PPP2R5D | protein phosphatase 2 regulatory subunit B'delta | 2 | 4 | ||||||||
MIRT536512 | KCTD15 | potassium channel tetramerization domain containing 15 | 2 | 2 | ||||||||
MIRT543793 | RALGAPB | Ral GTPase activating protein non-catalytic beta subunit | 2 | 2 | ||||||||
MIRT563977 | HCFC1 | host cell factor C1 | 2 | 2 | ||||||||
MIRT569472 | MAN2A2 | mannosidase alpha class 2A member 2 | 2 | 2 | ||||||||
MIRT570600 | NFIX | nuclear factor I X | 2 | 2 | ||||||||
MIRT571402 | MED4 | mediator complex subunit 4 | 2 | 2 | ||||||||
MIRT608418 | PPIC | peptidylprolyl isomerase C | 2 | 6 | ||||||||
MIRT608928 | REXO2 | RNA exonuclease 2 | 2 | 4 | ||||||||
MIRT609357 | ZNF664 | zinc finger protein 664 | 2 | 2 | ||||||||
MIRT611189 | WBSCR17 | polypeptide N-acetylgalactosaminyltransferase 17 | 2 | 4 | ||||||||
MIRT615266 | DPF2 | double PHD fingers 2 | 2 | 2 | ||||||||
MIRT615408 | VDAC2 | voltage dependent anion channel 2 | 2 | 2 | ||||||||
MIRT616323 | AGO3 | argonaute 3, RISC catalytic component | 2 | 2 | ||||||||
MIRT616566 | ZNF512B | zinc finger protein 512B | 2 | 2 | ||||||||
MIRT616745 | TAZ | tafazzin | 2 | 2 | ||||||||
MIRT617316 | MBOAT1 | membrane bound O-acyltransferase domain containing 1 | 2 | 2 | ||||||||
MIRT620030 | NFAM1 | NFAT activating protein with ITAM motif 1 | 2 | 2 | ||||||||
MIRT621166 | RTTN | rotatin | 2 | 2 | ||||||||
MIRT623501 | KCNQ3 | potassium voltage-gated channel subfamily Q member 3 | 2 | 2 | ||||||||
MIRT623524 | KCNK10 | potassium two pore domain channel subfamily K member 10 | 2 | 2 | ||||||||
MIRT629683 | TNFAIP8L1 | TNF alpha induced protein 8 like 1 | 2 | 2 | ||||||||
MIRT630795 | TGIF2 | TGFB induced factor homeobox 2 | 2 | 2 | ||||||||
MIRT634638 | HIP1 | huntingtin interacting protein 1 | 2 | 4 | ||||||||
MIRT636788 | RAB40B | RAB40B, member RAS oncogene family | 2 | 2 | ||||||||
MIRT640332 | DAAM2 | dishevelled associated activator of morphogenesis 2 | 2 | 2 | ||||||||
MIRT640557 | SMCR8 | Smith-Magenis syndrome chromosome region, candidate 8 | 2 | 2 | ||||||||
MIRT643319 | TMEM151B | transmembrane protein 151B | 2 | 2 | ||||||||
MIRT643991 | DUSP28 | dual specificity phosphatase 28 | 2 | 2 | ||||||||
MIRT644618 | CD300E | CD300e molecule | 2 | 2 | ||||||||
MIRT646445 | XRCC2 | X-ray repair cross complementing 2 | 2 | 2 | ||||||||
MIRT648020 | SLCO4C1 | solute carrier organic anion transporter family member 4C1 | 2 | 2 | ||||||||
MIRT648077 | ZMIZ2 | zinc finger MIZ-type containing 2 | 2 | 2 | ||||||||
MIRT649618 | ITPKC | inositol-trisphosphate 3-kinase C | 2 | 2 | ||||||||
MIRT650414 | ZNF442 | zinc finger protein 442 | 2 | 2 | ||||||||
MIRT650850 | SEMA4G | semaphorin 4G | 2 | 2 | ||||||||
MIRT654694 | PSMB5 | proteasome subunit beta 5 | 2 | 2 | ||||||||
MIRT655512 | PAIP2B | poly(A) binding protein interacting protein 2B | 2 | 2 | ||||||||
MIRT657620 | GRAP2 | GRB2-related adaptor protein 2 | 2 | 2 | ||||||||
MIRT658009 | GALNT10 | polypeptide N-acetylgalactosaminyltransferase 10 | 2 | 2 | ||||||||
MIRT658329 | FAM83F | family with sequence similarity 83 member F | 2 | 2 | ||||||||
MIRT658832 | SRCAP | Snf2 related CREBBP activator protein | 2 | 2 | ||||||||
MIRT658920 | DPY19L4 | dpy-19 like 4 | 2 | 2 | ||||||||
MIRT661058 | RPL18A | ribosomal protein L18a | 2 | 2 | ||||||||
MIRT662342 | MYLK3 | myosin light chain kinase 3 | 2 | 2 | ||||||||
MIRT663451 | FBXO2 | F-box protein 2 | 2 | 2 | ||||||||
MIRT676752 | SGTB | small glutamine rich tetratricopeptide repeat containing beta | 2 | 4 | ||||||||
MIRT684705 | LRRD1 | leucine rich repeats and death domain containing 1 | 2 | 2 | ||||||||
MIRT687247 | PDHB | pyruvate dehydrogenase E1 beta subunit | 2 | 2 | ||||||||
MIRT693881 | NT5C2 | 5'-nucleotidase, cytosolic II | 2 | 2 | ||||||||
MIRT693922 | HNRNPA1L2 | heterogeneous nuclear ribonucleoprotein A1-like 2 | 2 | 2 | ||||||||
MIRT695921 | ZNF174 | zinc finger protein 174 | 2 | 2 | ||||||||
MIRT702867 | HNRNPA1 | heterogeneous nuclear ribonucleoprotein A1 | 2 | 2 | ||||||||
MIRT708863 | TMSB4X | thymosin beta 4, X-linked | 2 | 2 | ||||||||
MIRT708936 | CRY2 | cryptochrome circadian clock 2 | 2 | 2 | ||||||||
MIRT709476 | FAXC | failed axon connections homolog | 2 | 2 | ||||||||
MIRT709752 | UBD | ubiquitin D | 2 | 2 | ||||||||
MIRT710128 | VANGL2 | VANGL planar cell polarity protein 2 | 2 | 2 | ||||||||
MIRT710274 | FAM107A | family with sequence similarity 107 member A | 2 | 2 | ||||||||
MIRT711146 | TMEM174 | transmembrane protein 174 | 2 | 2 | ||||||||
MIRT712582 | ATP2B4 | ATPase plasma membrane Ca2+ transporting 4 | 2 | 2 | ||||||||
MIRT712648 | TXNL4A | thioredoxin like 4A | 2 | 2 | ||||||||
MIRT713325 | TMEM44 | transmembrane protein 44 | 2 | 2 | ||||||||
MIRT713413 | PEX16 | peroxisomal biogenesis factor 16 | 2 | 2 | ||||||||
MIRT713891 | RNF19B | ring finger protein 19B | 2 | 2 | ||||||||
MIRT714549 | COL14A1 | collagen type XIV alpha 1 chain | 2 | 2 | ||||||||
MIRT714809 | ARHGEF19 | Rho guanine nucleotide exchange factor 19 | 2 | 2 | ||||||||
MIRT714840 | SCAMP2 | secretory carrier membrane protein 2 | 2 | 2 | ||||||||
MIRT715779 | DDX42 | DEAD-box helicase 42 | 2 | 2 | ||||||||
MIRT715795 | TBL3 | transducin beta like 3 | 2 | 2 | ||||||||
MIRT716088 | RNF150 | ring finger protein 150 | 2 | 2 | ||||||||
MIRT716712 | IMP4 | IMP4, U3 small nucleolar ribonucleoprotein | 2 | 2 | ||||||||
MIRT716737 | APOL6 | apolipoprotein L6 | 2 | 2 | ||||||||
MIRT717069 | MTMR6 | myotubularin related protein 6 | 2 | 2 | ||||||||
MIRT718185 | HLCS | holocarboxylase synthetase | 2 | 2 | ||||||||
MIRT719386 | SECTM1 | secreted and transmembrane 1 | 2 | 2 | ||||||||
MIRT720679 | SLC39A13 | solute carrier family 39 member 13 | 2 | 2 | ||||||||
MIRT721315 | FAM58A | cyclin Q | 2 | 2 | ||||||||
MIRT721396 | LDLRAD4 | low density lipoprotein receptor class A domain containing 4 | 2 | 2 | ||||||||
MIRT721896 | ITPR2 | inositol 1,4,5-trisphosphate receptor type 2 | 2 | 2 | ||||||||
MIRT722442 | ZBTB7B | zinc finger and BTB domain containing 7B | 2 | 2 | ||||||||
MIRT723009 | FADS1 | fatty acid desaturase 1 | 2 | 2 | ||||||||
MIRT723675 | CTC1 | CST telomere replication complex component 1 | 2 | 2 | ||||||||
MIRT723774 | ROBO4 | roundabout guidance receptor 4 | 2 | 2 | ||||||||
MIRT723814 | OR1L8 | olfactory receptor family 1 subfamily L member 8 | 2 | 2 | ||||||||
MIRT723959 | TMEM184A | transmembrane protein 184A | 2 | 2 | ||||||||
MIRT724449 | OPA3 | OPA3, outer mitochondrial membrane lipid metabolism regulator | 2 | 2 | ||||||||
MIRT724798 | C1D | C1D nuclear receptor corepressor | 2 | 2 | ||||||||
MIRT725626 | CAMKV | CaM kinase like vesicle associated | 2 | 2 |