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MIR4687 (microRNA 4687)

Identity

Alias_symbol (synonym)hsa-mir-4687
Other alias-
HGNC (Hugo) MIR4687
LocusID (NCBI) 100616453
Atlas_Id 69602
Location 11p15.4  [Link to chromosome band 11p15]
Location_base_pair Starts at 3856062 and ends at 3856141 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)MIR4687   41712
Cards
Entrez_Gene (NCBI)MIR4687  100616453  microRNA 4687
Aliases
GeneCards (Weizmann)MIR4687
Ensembl hg19 (Hinxton)ENSG00000263421 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263421 [Gene_View]  chr11:3856062-3856141 [Contig_View]  MIR4687 [Vega]
ICGC DataPortalENSG00000263421
TCGA cBioPortalMIR4687
AceView (NCBI)MIR4687
Genatlas (Paris)MIR4687
WikiGenes100616453
SOURCE (Princeton)MIR4687
Genetics Home Reference (NIH)MIR4687
miRBaseMIR4687
dbDEMCMIR4687
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4687  -     chr11:3856062-3856141 +  11p15.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4687  -     11p15.4   [Description]    (hg19-Feb_2009)
EnsemblMIR4687 - 11p15.4 [CytoView hg19]  MIR4687 - 11p15.4 [CytoView hg38]
Mapping of homologs : NCBIMIR4687 [Mapview hg19]  MIR4687 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4687
Alternative Splicing GalleryENSG00000263421
Gene ExpressionMIR4687 [ NCBI-GEO ]   MIR4687 [ EBI - ARRAY_EXPRESS ]   MIR4687 [ SEEK ]   MIR4687 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4687 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616453
GTEX Portal (Tissue expression)MIR4687
Human Protein AtlasENSG00000263421-MIR4687 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4687
DMDM Disease mutations100616453
Blocks (Seattle)MIR4687
Human Protein Atlas [tissue]ENSG00000263421-MIR4687 [tissue]
Protein Interaction databases
FunCoupENSG00000263421
BioGRIDMIR4687
STRING (EMBL)MIR4687
ZODIACMIR4687
Ontologies - Pathways
Huge Navigator MIR4687 [HugePedia]
snp3D : Map Gene to Disease100616453
BioCentury BCIQMIR4687
ClinGenMIR4687
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616453
Clinical trialMIR4687
Miscellaneous
canSAR (ICR)MIR4687 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4687
EVEXMIR4687
GoPubMedMIR4687
iHOPMIR4687
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 13:23:56 CET 2017

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