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MIR4711 (microRNA 4711)

Identity

Alias_symbol (synonym)hsa-mir-4711
Other alias-
HGNC (Hugo) MIR4711
LocusID (NCBI) 100616409
Atlas_Id 69625
Location 1p32.1  [Link to chromosome band 1p32]
Location_base_pair Starts at 59733227 and ends at 59733296 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)MIR4711   41847
Cards
Entrez_Gene (NCBI)MIR4711  100616409  microRNA 4711
Aliases
GeneCards (Weizmann)MIR4711
Ensembl hg19 (Hinxton)ENSG00000266150 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266150 [Gene_View]  chr1:59733227-59733296 [Contig_View]  MIR4711 [Vega]
ICGC DataPortalENSG00000266150
TCGA cBioPortalMIR4711
AceView (NCBI)MIR4711
Genatlas (Paris)MIR4711
WikiGenes100616409
SOURCE (Princeton)MIR4711
Genetics Home Reference (NIH)MIR4711
miRBaseMIR4711
dbDEMCMIR4711
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4711  -     chr1:59733227-59733296 -  1p32.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4711  -     1p32.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4711 - 1p32.1 [CytoView hg19]  MIR4711 - 1p32.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4711 [Mapview hg19]  MIR4711 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4711
Alternative Splicing GalleryENSG00000266150
Gene ExpressionMIR4711 [ NCBI-GEO ]   MIR4711 [ EBI - ARRAY_EXPRESS ]   MIR4711 [ SEEK ]   MIR4711 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4711 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616409
GTEX Portal (Tissue expression)MIR4711
Human Protein AtlasENSG00000266150-MIR4711 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4711
DMDM Disease mutations100616409
Blocks (Seattle)MIR4711
Human Protein Atlas [tissue]ENSG00000266150-MIR4711 [tissue]
Protein Interaction databases
FunCoupENSG00000266150
BioGRIDMIR4711
STRING (EMBL)MIR4711
ZODIACMIR4711
Ontologies - Pathways
Huge Navigator MIR4711 [HugePedia]
snp3D : Map Gene to Disease100616409
BioCentury BCIQMIR4711
ClinGenMIR4711
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616409
Clinical trialMIR4711
Miscellaneous
canSAR (ICR)MIR4711 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4711
EVEXMIR4711
GoPubMedMIR4711
iHOPMIR4711
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 13:01:39 CET 2017

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