Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR6882 (microRNA 6882)

Identity

Alias_symbol (synonym)hsa-mir-6882
Other alias
HGNC (Hugo) MIR6882
LocusID (NCBI) 102465531
Atlas_Id 70184
Location 15q24.1  [Link to chromosome band 15q24]
Location_base_pair Starts at 74840642 and ends at 74840707 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)MIR6882   49928
Cards
Entrez_Gene (NCBI)MIR6882  102465531  microRNA 6882
Aliaseshsa-mir-6882
GeneCards (Weizmann)MIR6882
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr15:74840642-74840707 [Contig_View]  MIR6882 [Vega]
TCGA cBioPortalMIR6882
AceView (NCBI)MIR6882
Genatlas (Paris)MIR6882
WikiGenes102465531
SOURCE (Princeton)MIR6882
Genetics Home Reference (NIH)MIR6882
miRBaseMIR6882
dbDEMCMIR6882
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6882  -     chr15:74840642-74840707 -  15q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6882  -     15q24.1   [Description]    (hg19-Feb_2009)
EnsemblMIR6882 - 15q24.1 [CytoView hg19]  MIR6882 - 15q24.1 [CytoView hg38]
Mapping of homologs : NCBIMIR6882 [Mapview hg19]  MIR6882 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR6882
Gene ExpressionMIR6882 [ NCBI-GEO ]   MIR6882 [ EBI - ARRAY_EXPRESS ]   MIR6882 [ SEEK ]   MIR6882 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6882 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102465531
GTEX Portal (Tissue expression)MIR6882
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6882
DMDM Disease mutations102465531
Blocks (Seattle)MIR6882
Protein Interaction databases
BioGRIDMIR6882
STRING (EMBL)MIR6882
ZODIACMIR6882
Ontologies - Pathways
Huge Navigator MIR6882 [HugePedia]
snp3D : Map Gene to Disease102465531
BioCentury BCIQMIR6882
ClinGenMIR6882
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102465531
Clinical trialMIR6882
Miscellaneous
canSAR (ICR)MIR6882 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6882
EVEXMIR6882
GoPubMedMIR6882
iHOPMIR6882
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 : Thu Nov 9 12:16:57 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.