MIR5047 (microRNA 5047) - Rat Genome Database

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Gene: MIR5047 (microRNA 5047) Homo sapiens
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Symbol: MIR5047
Name: microRNA 5047
RGD ID: 5133844
HGNC Page HGNC:41834
Description: microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]
Type: ncrna (Ensembl: miRNA)
RefSeq Status: PROVISIONAL
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381764,501,214 - 64,501,313 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1764,501,214 - 64,501,313 (-)EnsemblGRCh38hg38GRCh38
GRCh371762,497,332 - 62,497,431 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map17q23.3NCBI
HuRef1757,946,397 - 57,946,496 (-)NCBIHuRef
CHM1_11762,561,257 - 62,561,356 (-)NCBICHM1_1
T2T-CHM13v2.01765,370,970 - 65,371,069 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


References
Additional References at PubMed
PMID:16381832   PMID:21346006   PMID:37382256  


Genomics


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q23.3-24.1(chr17:64307125-64748462)x1 copy number loss See cases [RCV000135784] Chr17:64307125..64748462 [GRCh38]
Chr17:59738217..60175042 [NCBI36]
Chr17:17q23.3-24.1
uncertain significance
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1
pathogenic
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2
pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3
pathogenic
miRNA Target Status

Predicted Targets
Summary Value
Count of predictions:29387
Count of gene targets:12642
Count of transcripts:25682
Interacting mature miRNAs:hsa-miR-5047
Prediction methods:Microtar, Miranda, Pita, Pita,Microtar, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage
High
Medium 1 3 3 1 3 1 4 1 1
Low 1183 1056 852 131 451 55 1257 692 1052 42 457 801 76 495 783
Below cutoff 28 95 21 7 15 5 32 65 92 8 2 4 2 8 20

Sequence


RefSeq Acc Id: ENST00000579212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1764,501,214 - 64,501,313 (-)Ensembl
RefSeq Acc Id: NR_039969
RefSeq Status: PROVISIONAL
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381764,501,214 - 64,501,313 (-)NCBI
GRCh371762,497,332 - 62,497,431 (-)ENTREZGENE
HuRef1757,946,397 - 57,946,496 (-)ENTREZGENE
CHM1_11762,561,257 - 62,561,356 (-)NCBI
T2T-CHM13v2.01765,370,970 - 65,371,069 (-)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC MIR5047 COSMIC
Ensembl Genes ENSG00000284368 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000579212 ENTREZGENE
GTEx ENSG00000284368 GTEx
HGNC ID HGNC:41834 ENTREZGENE
Human Proteome Map MIR5047 Human Proteome Map
miRBase MI0017932 ENTREZGENE
NCBI Gene 100616408 ENTREZGENE
RNAcentral URS000075CFDE RNACentral
  URS000075DBE4 RNACentral