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MIR6087 (microRNA 6087)

Identity

Alias_symbol (synonym)hsa-mir-6087
Other alias
HGNC (Hugo) MIR6087
LocusID (NCBI) 102464835
Atlas_Id 77122
Location Xq22.3  [Link to chromosome band Xq22]
Location_base_pair Starts at 109054542 and ends at 109054590 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)MIR6087   50045
Cards
Entrez_Gene (NCBI)MIR6087  102464835  microRNA 6087
Aliaseshsa-mir-6087
GeneCards (Weizmann)MIR6087
Ensembl hg19 (Hinxton)ENSG00000275110 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275110 [Gene_View]  chrX:109054542-109054590 [Contig_View]  MIR6087 [Vega]
ICGC DataPortalENSG00000275110
TCGA cBioPortalMIR6087
AceView (NCBI)MIR6087
Genatlas (Paris)MIR6087
WikiGenes102464835
SOURCE (Princeton)MIR6087
Genetics Home Reference (NIH)MIR6087
miRBaseMIR6087
dbDEMCMIR6087
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6087  -     chrX:109054542-109054590 +  Xq22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6087  -     Xq22.3   [Description]    (hg19-Feb_2009)
EnsemblMIR6087 - Xq22.3 [CytoView hg19]  MIR6087 - Xq22.3 [CytoView hg38]
Mapping of homologs : NCBIMIR6087 [Mapview hg19]  MIR6087 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR6087
Alternative Splicing GalleryENSG00000275110
Gene ExpressionMIR6087 [ NCBI-GEO ]   MIR6087 [ EBI - ARRAY_EXPRESS ]   MIR6087 [ SEEK ]   MIR6087 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6087 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102464835
GTEX Portal (Tissue expression)MIR6087
Human Protein AtlasENSG00000275110-MIR6087 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6087
DMDM Disease mutations102464835
Blocks (Seattle)MIR6087
Human Protein Atlas [tissue]ENSG00000275110-MIR6087 [tissue]
Protein Interaction databases
FunCoupENSG00000275110
BioGRIDMIR6087
STRING (EMBL)MIR6087
ZODIACMIR6087
Ontologies - Pathways
Huge Navigator MIR6087 [HugePedia]
snp3D : Map Gene to Disease102464835
BioCentury BCIQMIR6087
ClinGenMIR6087
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102464835
Clinical trialMIR6087
Miscellaneous
canSAR (ICR)MIR6087 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6087
EVEXMIR6087
GoPubMedMIR6087
iHOPMIR6087
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 14:00:08 CET 2017

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