Human Gene MIR4722 (uc021tmp.1)
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Sequence and Links to Tools and Databases
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Primer design for this transcript
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
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Microarray Expression Data
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Orthologous Genes in Other Species
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Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Mouse | Rat | Zebrafish | D. melanogaster | C. elegans | S. cerevisiae |
No ortholog | No ortholog | No ortholog | No ortholog | No ortholog | No ortholog |
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Descriptions from all associated GenBank mRNAs
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AK092007 - Homo sapiens cDNA FLJ34688 fis, clone MESAN2000711. AX747306 - Sequence 831 from Patent EP1308459. FR773001 - Homo sapiens microRNA hsa-miR-4722-3p. HW799041 - WO 2014192907-A/147: Method for detecting miRNA used for differentiating disorders causing motor neuropathy. HZ481877 - JP 2015535430-A/2383: TERMINALLY MODIFIED RNA. HZ791808 - JP 2016504050-A/3553: SIGNAL-SENSOR POLYNUCLEOTIDES FOR THE ALTERATION OF CELLULAR PHENOTYPES. JC514540 - Sequence 4793 from Patent WO2014113089. LF160485 - JP 2016513950-A/551: Oligomers with improved off-target profile. LQ072128 - Sequence 2452 from Patent EP2964234. LZ208060 - WO 2017131208-A/14: Pharmaceutical composition for treatment and/or prevention of cancer. HZ409526 - JP 2015528002-A/2123: CHIRAL CONTROL. LG052860 - KR 1020150036642-A/2126: CHIRAL CONTROL. FR773002 - Homo sapiens microRNA hsa-miR-4722-5p. HZ481878 - JP 2015535430-A/2384: TERMINALLY MODIFIED RNA. HZ791809 - JP 2016504050-A/3554: SIGNAL-SENSOR POLYNUCLEOTIDES FOR THE ALTERATION OF CELLULAR PHENOTYPES. JC514541 - Sequence 4794 from Patent WO2014113089. LF160099 - JP 2016513950-A/165: Oligomers with improved off-target profile. LF632595 - WO 2016117582-A/24: miRNA biomarkers for mental disorders. LQ072129 - Sequence 2453 from Patent EP2964234. MA645629 - JP 2017113010-A/3553: SIGNAL-SENSOR POLYNUCLEOTIDES FOR THE ALTERATION OF CELLULAR PHENOTYPES. MA733513 - JP 2017140048-A/2383: TERMINALLY MODIFIED RNA. MA645630 - JP 2017113010-A/3554: SIGNAL-SENSOR POLYNUCLEOTIDES FOR THE ALTERATION OF CELLULAR PHENOTYPES. MA733514 - JP 2017140048-A/2384: TERMINALLY MODIFIED RNA. MA405639 - WO 2018155427-A/413: A probe with reduced false positive binding, a method to desing the probe, and the use thereof. MA405822 - WO 2018155427-A/596: A probe with reduced false positive binding, a method to desing the probe, and the use thereof. MP025569 - Sequence 14 from Patent EP3409281. MA802682 - JP 2018183181-A/3553: SIGNAL-SENSOR POLYNUCLEOTIDES FOR THE ALTERATION OF CELLULAR PHENOTYPES. MA806196 - WO 2018199275-A/456: Kit, device and method for detection of ovary tumor. MA802683 - JP 2018183181-A/3554: SIGNAL-SENSOR POLYNUCLEOTIDES FOR THE ALTERATION OF CELLULAR PHENOTYPES. MA805920 - WO 2018199275-A/180: Kit, device and method for detection of ovary tumor. MA806457 - WO 2018199275-A/717: Kit, device and method for detection of ovary tumor. MA822594 - WO 2019004436-A/407: Kit, device, and method for detection of lung cancer. MA822258 - WO 2019004436-A/71: Kit, device, and method for detection of lung cancer. MB406844 - WO 2019159884-A/334: Kit, device, and method for detection of dementia. MB407237 - WO 2019159884-A/727: Kit, device, and method for detection of dementia. MB472958 - WO 2019208671-A/357: Kit or device and method for detecting bladder cancer. MB472723 - WO 2019208671-A/122: Kit or device and method for detecting bladder cancer.
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Other Names for This Gene
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Alternate Gene Symbols: NR_039873 UCSC ID: uc021tmp.1 RefSeq Accession: NR_039873
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Gene Model Information
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category:
| noncoding
| nonsense-mediated-decay:
| no
| RNA accession:
| NR_039873.1
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exon count:
| 1 | CDS single in 3' UTR:
| no
| RNA size:
| 60 |
ORF size:
| 0 | CDS single in intron:
| no
| Alignment % ID:
| 100.00 |
txCdsPredict score:
| 0.00 | frame shift in genome:
| no
| % Coverage:
| 100.00 |
has start codon:
| no
| stop codon in genome:
| no
| # of Alignments:
| 1 |
has end codon:
| no
| retained intron:
| no
| # AT/AC introns
| 0 |
selenocysteine:
| no
| end bleed into intron:
| 0 | # strange splices:
| 0 |
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Click here
for a detailed description of the fields of the table above.
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Methods, Credits, and Use Restrictions
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Click here
for details on how this gene model was made and data restrictions if any.
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