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MIR587 (microRNA 587)

Identity

Alias (NCBI)MIRN587
hsa-mir-587
HGNC (Hugo) MIR587
HGNC Alias symbhsa-mir-587
HGNC Previous nameMIRN587
LocusID (NCBI) 693172
Atlas_Id 55717
Location 6q21  [Link to chromosome band 6q21]
Location_base_pair Starts at 106784125 and ends at 106784220 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 



External links

Nomenclature
HGNC (Hugo)MIR587   32843
Cards
Entrez_Gene (NCBI)MIR587  693172  microRNA 587
AliasesMIRN587; hsa-mir-587
GeneCards (Weizmann)MIR587
Ensembl hg19 (Hinxton)ENSG00000207577 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207577 [Gene_View]  ENSG00000207577 [Sequence]  chr6:106784125-106784220 [Contig_View]  MIR587 [Vega]
ICGC DataPortalENSG00000207577
TCGA cBioPortalMIR587
AceView (NCBI)MIR587
Genatlas (Paris)MIR587
WikiGenes693172
SOURCE (Princeton)MIR587
Genetics Home Reference (NIH)MIR587
miRBaseMIR587
dbDEMCMIR587
Genomic and cartography
GoldenPath hg38 (UCSC)MIR587  -     chr6:106784125-106784220 +  6q21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR587  -     6q21   [Description]    (hg19-Feb_2009)
GoldenPathMIR587 - 6q21 [CytoView hg19]  MIR587 - 6q21 [CytoView hg38]
ImmunoBaseENSG00000207577
genome Data Viewer NCBIMIR587 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR587
Alternative Splicing GalleryENSG00000207577
Gene ExpressionMIR587 [ NCBI-GEO ]   MIR587 [ EBI - ARRAY_EXPRESS ]   MIR587 [ SEEK ]   MIR587 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR587 [ Firebrowse - Broad ]
GenevisibleExpression of MIR587 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)693172
GTEX Portal (Tissue expression)MIR587
Human Protein AtlasENSG00000207577-MIR587 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR587
DMDM Disease mutations693172
Blocks (Seattle)MIR587
Human Protein Atlas [tissue]ENSG00000207577-MIR587 [tissue]
Protein Interaction databases
FunCoupENSG00000207577
BioGRIDMIR587
STRING (EMBL)MIR587
ZODIACMIR587
Ontologies - Pathways
Huge Navigator MIR587 [HugePedia]
snp3D : Map Gene to Disease693172
BioCentury BCIQMIR587
ClinGenMIR587
Clinical trials, drugs, therapy
Protein Interactions : CTD693172
Pharm GKB GenePA164722884
Clinical trialMIR587
Miscellaneous
canSAR (ICR)MIR587 (select the gene name)
HarmonizomeMIR587
DataMed IndexMIR587
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR587
EVEXMIR587
GoPubMedMIR587
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Sep 14 14:22:00 CEST 2020

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