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MIR4723 (microRNA 4723)

Identity

Alias_symbol (synonym)hsa-mir-4723
Other aliasmir-4723
HGNC (Hugo) MIR4723
LocusID (NCBI) 100616388
Atlas_Id 54883
Location 17q11.2  [Link to chromosome band 17q11]
Location_base_pair Starts at 28360654 and ends at 28360734 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)MIR4723   41660
Cards
Entrez_Gene (NCBI)MIR4723  100616388  microRNA 4723
Aliasesmir-4723
GeneCards (Weizmann)MIR4723
Ensembl hg19 (Hinxton)ENSG00000264302 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264302 [Gene_View]  chr17:28360654-28360734 [Contig_View]  MIR4723 [Vega]
ICGC DataPortalENSG00000264302
TCGA cBioPortalMIR4723
AceView (NCBI)MIR4723
Genatlas (Paris)MIR4723
WikiGenes100616388
SOURCE (Princeton)MIR4723
Genetics Home Reference (NIH)MIR4723
miRBaseMIR4723
dbDEMCMIR4723
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4723  -     chr17:28360654-28360734 +  17q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4723  -     17q11.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4723 - 17q11.2 [CytoView hg19]  MIR4723 - 17q11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4723 [Mapview hg19]  MIR4723 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611394
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4723
Alternative Splicing GalleryENSG00000264302
Gene ExpressionMIR4723 [ NCBI-GEO ]   MIR4723 [ EBI - ARRAY_EXPRESS ]   MIR4723 [ SEEK ]   MIR4723 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4723 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616388
GTEX Portal (Tissue expression)MIR4723
Human Protein AtlasENSG00000264302-MIR4723 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4723
DMDM Disease mutations100616388
Blocks (Seattle)MIR4723
Human Protein Atlas [tissue]ENSG00000264302-MIR4723 [tissue]
Protein Interaction databases
FunCoupENSG00000264302
BioGRIDMIR4723
STRING (EMBL)MIR4723
ZODIACMIR4723
Ontologies - Pathways
Huge Navigator MIR4723 [HugePedia]
snp3D : Map Gene to Disease100616388
BioCentury BCIQMIR4723
ClinGenMIR4723
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616388
Clinical trialMIR4723
Miscellaneous
canSAR (ICR)MIR4723 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4723
EVEXMIR4723
GoPubMedMIR4723
iHOPMIR4723
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 : Tue Nov 21 14:23:36 CET 2017

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