MIR4732 (microRNA 4732) - Rat Genome Database

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Gene: MIR4732 (microRNA 4732) Homo sapiens
Analyze
Symbol: MIR4732
Name: microRNA 4732
RGD ID: 5134065
HGNC Page HGNC:41639
Description: Located in extracellular space.
Type: ncrna (Ensembl: miRNA)
RefSeq Status: PROVISIONAL
Previously known as: mir-4732
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381728,861,655 - 28,861,730 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1728,861,655 - 28,861,730 (-)EnsemblGRCh38hg38GRCh38
GRCh371727,188,673 - 27,188,748 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map17q11.2NCBI
HuRef1723,396,963 - 23,397,038 (-)NCBIHuRef
CHM1_11727,251,187 - 27,251,262 (-)NCBICHM1_1
T2T-CHM13v2.01729,804,428 - 29,804,503 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:16381832   PMID:21037258   PMID:21199797   PMID:25203061   PMID:26646931   PMID:29955039   PMID:30701690   PMID:33910598   PMID:33916069   PMID:34758406   PMID:35388387   PMID:37125501  
PMID:38654325  


Genomics


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q11.2(chr17:28283125-28904397)x3 copy number gain See cases [RCV000136494] Chr17:28283125..28904397 [GRCh38]
Chr17:26610151..27231415 [GRCh37]
Chr17:23634278..24255541 [NCBI36]
Chr17:17q11.2		 benign
GRCh38/hg38 17q11.2(chr17:28757283-29216419)x3 copy number gain See cases [RCV000142450] Chr17:28757283..29216419 [GRCh38]
Chr17:27084301..27543437 [GRCh37]
Chr17:24108428..24567563 [NCBI36]
Chr17:17q11.2		 uncertain significance
miRNA Target Status

Predicted Targets
Summary Value
Count of predictions:31312
Count of gene targets:12003
Count of transcripts:24019
Interacting mature miRNAs:hsa-miR-4732-3p, hsa-miR-4732-5p
Prediction methods:Microtar, Miranda, Pita, 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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1298406BP16_HBlood pressure QTL 16 (human)0.0004Blood pressurehypertension susceptibility171477864740778647Human


Expression

RNA-SEQ Expression


Sequence


Ensembl Acc Id: ENST00000581873
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1728,861,655 - 28,861,730 (-)Ensembl
RefSeq Acc Id: NR_039885
RefSeq Status: PROVISIONAL
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381728,861,655 - 28,861,730 (-)NCBI
GRCh371727,188,673 - 27,188,748 (-)ENTREZGENE
HuRef1723,396,963 - 23,397,038 (-)ENTREZGENE
CHM1_11727,251,187 - 27,251,262 (-)NCBI
T2T-CHM13v2.01729,804,428 - 29,804,503 (-)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC MIR4732 COSMIC
Ensembl Genes ENSG00000284085 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000581873 ENTREZGENE
GTEx ENSG00000284085 GTEx
HGNC ID HGNC:41639 ENTREZGENE
Human Proteome Map MIR4732 Human Proteome Map
miRBase MI0017369 ENTREZGENE
NCBI Gene 100616385 ENTREZGENE
RNAcentral URS00001A122A RNACentral
  URS0000240326 RNACentral
  URS000075B046 RNACentral