Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR8071-2 (microRNA 8071-2)

Identity

Alias_symbol (synonym)hsa-mir-8071-2
Other alias
HGNC (Hugo) MIR8071-2
LocusID (NCBI) 102466889
Atlas_Id 70272
Location 14q32.33  [Link to chromosome band 14q32]
Location_base_pair Starts at 105621116 and ends at 105621180 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)MIR8071-2   49958
Cards
Entrez_Gene (NCBI)MIR8071-2  102466889  microRNA 8071-2
Aliaseshsa-mir-8071-2
GeneCards (Weizmann)MIR8071-2
Ensembl hg19 (Hinxton)ENSG00000277030 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277030 [Gene_View]  chr14:105621116-105621180 [Contig_View]  MIR8071-2 [Vega]
ICGC DataPortalENSG00000277030
TCGA cBioPortalMIR8071-2
AceView (NCBI)MIR8071-2
Genatlas (Paris)MIR8071-2
WikiGenes102466889
SOURCE (Princeton)MIR8071-2
Genetics Home Reference (NIH)MIR8071-2
miRBaseMIR8071-2
dbDEMCMIR8071-2
Genomic and cartography
GoldenPath hg38 (UCSC)MIR8071-2  -     chr14:105621116-105621180 +  14q32.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR8071-2  -     14q32.33   [Description]    (hg19-Feb_2009)
EnsemblMIR8071-2 - 14q32.33 [CytoView hg19]  MIR8071-2 - 14q32.33 [CytoView hg38]
Mapping of homologs : NCBIMIR8071-2 [Mapview hg19]  MIR8071-2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000014 NT_187600
Consensus coding sequences : CCDS (NCBI)MIR8071-2
Alternative Splicing GalleryENSG00000277030
Gene ExpressionMIR8071-2 [ NCBI-GEO ]   MIR8071-2 [ EBI - ARRAY_EXPRESS ]   MIR8071-2 [ SEEK ]   MIR8071-2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR8071-2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102466889
GTEX Portal (Tissue expression)MIR8071-2
Human Protein AtlasENSG00000277030-MIR8071-2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR8071-2
DMDM Disease mutations102466889
Blocks (Seattle)MIR8071-2
Human Protein Atlas [tissue]ENSG00000277030-MIR8071-2 [tissue]
Protein Interaction databases
FunCoupENSG00000277030
BioGRIDMIR8071-2
STRING (EMBL)MIR8071-2
ZODIACMIR8071-2
Ontologies - Pathways
Huge Navigator MIR8071-2 [HugePedia]
snp3D : Map Gene to Disease102466889
BioCentury BCIQMIR8071-2
ClinGenMIR8071-2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102466889
Clinical trialMIR8071-2
Miscellaneous
canSAR (ICR)MIR8071-2 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR8071-2
EVEXMIR8071-2
GoPubMedMIR8071-2
iHOPMIR8071-2
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 Nov 9 12:17:16 CET 2017

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