Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

MIR6855 (microRNA 6855)

Identity

Alias_symbol (synonym)hsa-mir-6855
Other alias
HGNC (Hugo) MIR6855
LocusID (NCBI) 102466750
Atlas_Id 70155
Location 9q34.11  [Link to chromosome band 9q34]
Location_base_pair Starts at 132631884 and ends at 132631950 bp from pter ( according to hg19-Feb_2009)

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)MIR6855   50061
Cards
Entrez_Gene (NCBI)MIR6855  102466750  microRNA 6855
Aliaseshsa-mir-6855
GeneCards (Weizmann)MIR6855
Ensembl hg19 (Hinxton) [Gene_View]  chr9:132631884-132631950 [Contig_View]  MIR6855 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:132631884-132631950 [Contig_View]  MIR6855 [Vega]
TCGA cBioPortalMIR6855
AceView (NCBI)MIR6855
Genatlas (Paris)MIR6855
WikiGenes102466750
SOURCE (Princeton)MIR6855
Genetics Home Reference (NIH)MIR6855
miRBaseMIR6855
dbDEMCMIR6855
Genomic and cartography
GoldenPath hg19 (UCSC)MIR6855  -     chr9:132631884-132631950 +  9q34.11   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR6855  -     9q34.11   [Description]    (hg38-Dec_2013)
EnsemblMIR6855 - 9q34.11 [CytoView hg19]  MIR6855 - 9q34.11 [CytoView hg38]
Mapping of homologs : NCBIMIR6855 [Mapview hg19]  MIR6855 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_008470 NW_004929366
Consensus coding sequences : CCDS (NCBI)MIR6855
Gene ExpressionMIR6855 [ NCBI-GEO ]   MIR6855 [ EBI - ARRAY_EXPRESS ]   MIR6855 [ SEEK ]   MIR6855 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6855 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102466750
GTEX Portal (Tissue expression)MIR6855
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6855
DMDM Disease mutations102466750
Blocks (Seattle)MIR6855
Protein Interaction databases
BioGRIDMIR6855
STRING (EMBL)MIR6855
ZODIACMIR6855
Ontologies - Pathways
Huge Navigator MIR6855 [HugePedia]
snp3D : Map Gene to Disease102466750
BioCentury BCIQMIR6855
ClinGenMIR6855
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102466750
Clinical trialMIR6855
Miscellaneous
canSAR (ICR)MIR6855 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6855
EVEXMIR6855
GoPubMedMIR6855
iHOPMIR6855
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 Mar 14 12:32:40 CET 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.