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MIR6766 (microRNA 6766)

Identity

Alias (NCBI)hsa-mir-6766
HGNC (Hugo) MIR6766
HGNC Alias symbhsa-mir-6766
LocusID (NCBI) 102466983
Atlas_Id 70065
Location 15q26.1  [Link to chromosome band 15q26]
Location_base_pair Starts at 89326739 and ends at 89326810 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)MIR6766   49941
Cards
Entrez_Gene (NCBI)MIR6766  102466983  microRNA 6766
Aliaseshsa-mir-6766
GeneCards (Weizmann)MIR6766
Ensembl hg19 (Hinxton)ENSG00000275101 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275101 [Gene_View]  ENSG00000275101 [Sequence]  chr15:89326739-89326810 [Contig_View]  MIR6766 [Vega]
ICGC DataPortalENSG00000275101
TCGA cBioPortalMIR6766
AceView (NCBI)MIR6766
Genatlas (Paris)MIR6766
WikiGenes102466983
SOURCE (Princeton)MIR6766
Genetics Home Reference (NIH)MIR6766
miRBaseMIR6766
dbDEMCMIR6766
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6766  -     chr15:89326739-89326810 -  15q26.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6766  -     15q26.1   [Description]    (hg19-Feb_2009)
GoldenPathMIR6766 - 15q26.1 [CytoView hg19]  MIR6766 - 15q26.1 [CytoView hg38]
ImmunoBaseENSG00000275101
genome Data Viewer NCBIMIR6766 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR6766
Alternative Splicing GalleryENSG00000275101
Gene ExpressionMIR6766 [ NCBI-GEO ]   MIR6766 [ EBI - ARRAY_EXPRESS ]   MIR6766 [ SEEK ]   MIR6766 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6766 [ Firebrowse - Broad ]
GenevisibleExpression of MIR6766 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)102466983
GTEX Portal (Tissue expression)MIR6766
Human Protein AtlasENSG00000275101-MIR6766 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6766
DMDM Disease mutations102466983
Blocks (Seattle)MIR6766
Human Protein Atlas [tissue]ENSG00000275101-MIR6766 [tissue]
Protein Interaction databases
FunCoupENSG00000275101
BioGRIDMIR6766
STRING (EMBL)MIR6766
ZODIACMIR6766
Ontologies - Pathways
Huge Navigator MIR6766 [HugePedia]
snp3D : Map Gene to Disease102466983
BioCentury BCIQMIR6766
ClinGenMIR6766
Clinical trials, drugs, therapy
Protein Interactions : CTD102466983
Clinical trialMIR6766
Miscellaneous
canSAR (ICR)MIR6766 (select the gene name)
HarmonizomeMIR6766
DataMed IndexMIR6766
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6766
EVEXMIR6766
GoPubMedMIR6766
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 : Thu Jul 16 16:17:16 CEST 2020

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