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MIR6832 (microRNA 6832)

Identity

Alias (NCBI)hsa-mir-6832
HGNC (Hugo) MIR6832
HGNC Alias symbhsa-mir-6832
LocusID (NCBI) 102466745
Atlas_Id 70132
Location 6p21.33  [Link to chromosome band 6p21]
Location_base_pair Starts at 31633787 and ends at 31633858 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)MIR6832   50140
Cards
Entrez_Gene (NCBI)MIR6832  102466745  microRNA 6832
Aliaseshsa-mir-6832
GeneCards (Weizmann)MIR6832
Ensembl hg19 (Hinxton)ENSG00000274494 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000274494 [Gene_View]  ENSG00000274494 [Sequence]  chr6:31633787-31633858 [Contig_View]  MIR6832 [Vega]
ICGC DataPortalENSG00000274494
TCGA cBioPortalMIR6832
AceView (NCBI)MIR6832
Genatlas (Paris)MIR6832
WikiGenes102466745
SOURCE (Princeton)MIR6832
Genetics Home Reference (NIH)MIR6832
miRBaseMIR6832
dbDEMCMIR6832
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6832  -     chr6:31633787-31633858 +  6p21.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6832  -     6p21.33   [Description]    (hg19-Feb_2009)
GoldenPathMIR6832 - 6p21.33 [CytoView hg19]  MIR6832 - 6p21.33 [CytoView hg38]
ImmunoBaseENSG00000274494
genome Data Viewer NCBIMIR6832 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000006 NT_113891 NT_167245 NT_167246 NT_167247 NT_167248 NT_167249
Consensus coding sequences : CCDS (NCBI)MIR6832
Alternative Splicing GalleryENSG00000274494
Gene ExpressionMIR6832 [ NCBI-GEO ]   MIR6832 [ EBI - ARRAY_EXPRESS ]   MIR6832 [ SEEK ]   MIR6832 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6832 [ Firebrowse - Broad ]
GenevisibleExpression of MIR6832 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)102466745
GTEX Portal (Tissue expression)MIR6832
Human Protein AtlasENSG00000274494-MIR6832 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6832
DMDM Disease mutations102466745
Blocks (Seattle)MIR6832
Human Protein Atlas [tissue]ENSG00000274494-MIR6832 [tissue]
Protein Interaction databases
FunCoupENSG00000274494
BioGRIDMIR6832
STRING (EMBL)MIR6832
ZODIACMIR6832
Ontologies - Pathways
Huge Navigator MIR6832 [HugePedia]
snp3D : Map Gene to Disease102466745
BioCentury BCIQMIR6832
ClinGenMIR6832
Clinical trials, drugs, therapy
Protein Interactions : CTD102466745
Clinical trialMIR6832
Miscellaneous
canSAR (ICR)MIR6832 (select the gene name)
HarmonizomeMIR6832
DataMed IndexMIR6832
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6832
EVEXMIR6832
GoPubMedMIR6832
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Aug 22 19:27:22 CEST 2020

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