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MIR6779 (microRNA 6779)

Identity

Alias (NCBI)hsa-mir-6779
HGNC (Hugo) MIR6779
HGNC Alias symbhsa-mir-6779
LocusID (NCBI) 102465467
Atlas_Id 70079
Location 17q12  [Link to chromosome band 17q12]
Location_base_pair Starts at 38914979 and ends at 38915042 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)MIR6779   50148
Cards
Entrez_Gene (NCBI)MIR6779    microRNA 6779
Aliaseshsa-mir-6779
GeneCards (Weizmann)MIR6779
Ensembl hg19 (Hinxton)ENSG00000277057 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277057 [Gene_View]  ENSG00000277057 [Sequence]  chr17:38914979-38915042 [Contig_View]  MIR6779 [Vega]
ICGC DataPortalENSG00000277057
TCGA cBioPortalMIR6779
AceView (NCBI)MIR6779
Genatlas (Paris)MIR6779
SOURCE (Princeton)MIR6779
Genetics Home Reference (NIH)MIR6779
miRBaseMIR6779
dbDEMCMIR6779
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6779  -     chr17:38914979-38915042 +  17q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6779  -     17q12   [Description]    (hg19-Feb_2009)
GoldenPathMIR6779 - 17q12 [CytoView hg19]  MIR6779 - 17q12 [CytoView hg38]
ImmunoBaseENSG00000277057
genome Data Viewer NCBIMIR6779 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR6779
Alternative Splicing GalleryENSG00000277057
Gene ExpressionMIR6779 [ NCBI-GEO ]   MIR6779 [ EBI - ARRAY_EXPRESS ]   MIR6779 [ SEEK ]   MIR6779 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6779 [ Firebrowse - Broad ]
GenevisibleExpression of MIR6779 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)102465467
GTEX Portal (Tissue expression)MIR6779
Human Protein AtlasENSG00000277057-MIR6779 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6779
Blocks (Seattle)MIR6779
Human Protein Atlas [tissue]ENSG00000277057-MIR6779 [tissue]
Protein Interaction databases
BioGRIDMIR6779
STRING (EMBL)MIR6779
ZODIACMIR6779
Ontologies - Pathways
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6779
EVEXMIR6779
GoPubMedMIR6779
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 : Sat Dec 5 17:16:48 CET 2020

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