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MIR7159 (microRNA 7159)

Identity

Alias_symbol (synonym)hsa-mir-7159
Other alias
HGNC (Hugo) MIR7159
LocusID (NCBI) 102466816
Atlas_Id 70214
Location 6p21.31  [Link to chromosome band 6p21]
Location_base_pair Starts at 33899135 and ends at 33899200 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)MIR7159   49978
Cards
Entrez_Gene (NCBI)MIR7159  102466816  microRNA 7159
Aliaseshsa-mir-7159
GeneCards (Weizmann)MIR7159
Ensembl hg19 (Hinxton)ENSG00000276824 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000276824 [Gene_View]  ENSG00000276824 [Sequence]  chr6:33899135-33899200 [Contig_View]  MIR7159 [Vega]
ICGC DataPortalENSG00000276824
TCGA cBioPortalMIR7159
AceView (NCBI)MIR7159
Genatlas (Paris)MIR7159
WikiGenes102466816
SOURCE (Princeton)MIR7159
Genetics Home Reference (NIH)MIR7159
miRBaseMIR7159
dbDEMCMIR7159
Genomic and cartography
GoldenPath hg38 (UCSC)MIR7159  -     chr6:33899135-33899200 +  6p21.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR7159  -     6p21.31   [Description]    (hg19-Feb_2009)
EnsemblMIR7159 - 6p21.31 [CytoView hg19]  MIR7159 - 6p21.31 [CytoView hg38]
Mapping of homologs : NCBIMIR7159 [Mapview hg19]  MIR7159 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR7159
Alternative Splicing GalleryENSG00000276824
Gene ExpressionMIR7159 [ NCBI-GEO ]   MIR7159 [ EBI - ARRAY_EXPRESS ]   MIR7159 [ SEEK ]   MIR7159 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR7159 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102466816
GTEX Portal (Tissue expression)MIR7159
Human Protein AtlasENSG00000276824-MIR7159 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR7159
DMDM Disease mutations102466816
Blocks (Seattle)MIR7159
Human Protein Atlas [tissue]ENSG00000276824-MIR7159 [tissue]
Protein Interaction databases
FunCoupENSG00000276824
BioGRIDMIR7159
STRING (EMBL)MIR7159
ZODIACMIR7159
Ontologies - Pathways
Huge Navigator MIR7159 [HugePedia]
snp3D : Map Gene to Disease102466816
BioCentury BCIQMIR7159
ClinGenMIR7159
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102466816
Clinical trialMIR7159
Miscellaneous
canSAR (ICR)MIR7159 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR7159
EVEXMIR7159
GoPubMedMIR7159
iHOPMIR7159
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 : Mon Jul 30 14:17:35 CEST 2018

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