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MIR3687-2 (microRNA 3687-2)

Identity

Other aliashsa-mir-3687-2
HGNC (Hugo) MIR3687-2
LocusID (NCBI) 103504728
Atlas_Id 76786
Location 21p11.2  [Link to chromosome band 21p11]
Location_base_pair Starts at 8208844 and ends at 8208904 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)MIR3687-2   50835
Cards
Entrez_Gene (NCBI)MIR3687-2  103504728  microRNA 3687-2
Aliaseshsa-mir-3687-2
GeneCards (Weizmann)MIR3687-2
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr21:8208844-8208904 [Contig_View]  MIR3687-2 [Vega]
TCGA cBioPortalMIR3687-2
AceView (NCBI)MIR3687-2
Genatlas (Paris)MIR3687-2
WikiGenes103504728
SOURCE (Princeton)MIR3687-2
Genetics Home Reference (NIH)MIR3687-2
miRBaseMIR3687-2
dbDEMCMIR3687-2
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3687-2  -     chr21:8208844-8208904 +  21p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3687-2  -     21p11.2   [Description]    (hg19-Feb_2009)
EnsemblMIR3687-2 - 21p11.2 [CytoView hg19]  MIR3687-2 - 21p11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR3687-2 [Mapview hg19]  MIR3687-2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3687-2
Gene ExpressionMIR3687-2 [ NCBI-GEO ]   MIR3687-2 [ EBI - ARRAY_EXPRESS ]   MIR3687-2 [ SEEK ]   MIR3687-2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3687-2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)103504728
GTEX Portal (Tissue expression)MIR3687-2
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3687-2
DMDM Disease mutations103504728
Blocks (Seattle)MIR3687-2
Protein Interaction databases
BioGRIDMIR3687-2
STRING (EMBL)MIR3687-2
ZODIACMIR3687-2
Ontologies - Pathways
Huge Navigator MIR3687-2 [HugePedia]
snp3D : Map Gene to Disease103504728
BioCentury BCIQMIR3687-2
ClinGenMIR3687-2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD103504728
Clinical trialMIR3687-2
Miscellaneous
canSAR (ICR)MIR3687-2 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3687-2
EVEXMIR3687-2
GoPubMedMIR3687-2
iHOPMIR3687-2
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 : Thu Nov 9 12:13:52 CET 2017

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