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MIR2113 (microRNA 2113)

Identity

Alias_symbol (synonym)hsa-mir-2113
Other alias
HGNC (Hugo) MIR2113
LocusID (NCBI) 100302164
Atlas_Id 69113
Location 6q16.1  [Link to chromosome band 6q16]
Location_base_pair Starts at 98024531 and ends at 98024619 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)MIR2113   37058
Cards
Entrez_Gene (NCBI)MIR2113  100302164  microRNA 2113
Aliaseshsa-mir-2113
GeneCards (Weizmann)MIR2113
Ensembl hg19 (Hinxton)ENSG00000238367 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000238367 [Gene_View]  ENSG00000238367 [Sequence]  chr6:98024531-98024619 [Contig_View]  MIR2113 [Vega]
ICGC DataPortalENSG00000238367
TCGA cBioPortalMIR2113
AceView (NCBI)MIR2113
Genatlas (Paris)MIR2113
WikiGenes100302164
SOURCE (Princeton)MIR2113
Genetics Home Reference (NIH)MIR2113
miRBaseMIR2113
dbDEMCMIR2113
Genomic and cartography
GoldenPath hg38 (UCSC)MIR2113  -     chr6:98024531-98024619 +  6q16.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR2113  -     6q16.1   [Description]    (hg19-Feb_2009)
EnsemblMIR2113 - 6q16.1 [CytoView hg19]  MIR2113 - 6q16.1 [CytoView hg38]
Mapping of homologs : NCBIMIR2113 [Mapview hg19]  MIR2113 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR2113
Alternative Splicing GalleryENSG00000238367
Gene ExpressionMIR2113 [ NCBI-GEO ]   MIR2113 [ EBI - ARRAY_EXPRESS ]   MIR2113 [ SEEK ]   MIR2113 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR2113 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100302164
GTEX Portal (Tissue expression)MIR2113
Human Protein AtlasENSG00000238367-MIR2113 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR2113
DMDM Disease mutations100302164
Blocks (Seattle)MIR2113
Human Protein Atlas [tissue]ENSG00000238367-MIR2113 [tissue]
Protein Interaction databases
FunCoupENSG00000238367
BioGRIDMIR2113
STRING (EMBL)MIR2113
ZODIACMIR2113
Ontologies - Pathways
Huge Navigator MIR2113 [HugePedia]
snp3D : Map Gene to Disease100302164
BioCentury BCIQMIR2113
ClinGenMIR2113
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100302164
Chemical/Pharm GKB GenePA164722594
Clinical trialMIR2113
Miscellaneous
canSAR (ICR)MIR2113 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR2113
EVEXMIR2113
GoPubMedMIR2113
iHOPMIR2113
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:13:23 CEST 2018

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