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MIR5011 (microRNA 5011)

Identity

Alias_symbol (synonym)hsa-mir-5011
Other alias-
HGNC (Hugo) MIR5011
LocusID (NCBI) 100847002
Atlas_Id 69737
Location 18q22.1  [Link to chromosome band 18q22]
Location_base_pair Starts at 67081584 and ends at 67081686 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)MIR5011   43496
Cards
Entrez_Gene (NCBI)MIR5011  100847002  microRNA 5011
Aliases
GeneCards (Weizmann)MIR5011
Ensembl hg19 (Hinxton)ENSG00000263354 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263354 [Gene_View]  chr18:67081584-67081686 [Contig_View]  MIR5011 [Vega]
ICGC DataPortalENSG00000263354
TCGA cBioPortalMIR5011
AceView (NCBI)MIR5011
Genatlas (Paris)MIR5011
WikiGenes100847002
SOURCE (Princeton)MIR5011
Genetics Home Reference (NIH)MIR5011
miRBaseMIR5011
dbDEMCMIR5011
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5011  -     chr18:67081584-67081686 +  18q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5011  -     18q22.1   [Description]    (hg19-Feb_2009)
EnsemblMIR5011 - 18q22.1 [CytoView hg19]  MIR5011 - 18q22.1 [CytoView hg38]
Mapping of homologs : NCBIMIR5011 [Mapview hg19]  MIR5011 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5011
Alternative Splicing GalleryENSG00000263354
Gene ExpressionMIR5011 [ NCBI-GEO ]   MIR5011 [ EBI - ARRAY_EXPRESS ]   MIR5011 [ SEEK ]   MIR5011 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5011 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847002
GTEX Portal (Tissue expression)MIR5011
Human Protein AtlasENSG00000263354-MIR5011 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5011
DMDM Disease mutations100847002
Blocks (Seattle)MIR5011
Human Protein Atlas [tissue]ENSG00000263354-MIR5011 [tissue]
Protein Interaction databases
FunCoupENSG00000263354
BioGRIDMIR5011
STRING (EMBL)MIR5011
ZODIACMIR5011
Ontologies - Pathways
Huge Navigator MIR5011 [HugePedia]
snp3D : Map Gene to Disease100847002
BioCentury BCIQMIR5011
ClinGenMIR5011
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847002
Clinical trialMIR5011
Miscellaneous
canSAR (ICR)MIR5011 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5011
EVEXMIR5011
GoPubMedMIR5011
iHOPMIR5011
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 : Tue Nov 21 13:37:48 CET 2017

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