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MIR5696 (microRNA 5696)

Identity

Alias_symbol (synonym)hsa-mir-5696
Other alias-
HGNC (Hugo) MIR5696
LocusID (NCBI) 100847007
Atlas_Id 69892
Location 2q11.2  [Link to chromosome band 2q11]
Location_base_pair Starts at 101925912 and ends at 101925996 bp from pter ( according to hg19-Feb_2009)

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)MIR5696   43516
Cards
Entrez_Gene (NCBI)MIR5696  100847007  microRNA 5696
Aliases
GeneCards (Weizmann)MIR5696
Ensembl hg19 (Hinxton)ENSG00000264857 [Gene_View]  chr2:101925912-101925996 [Contig_View]  MIR5696 [Vega]
Ensembl hg38 (Hinxton)ENSG00000264857 [Gene_View]  chr2:101925912-101925996 [Contig_View]  MIR5696 [Vega]
ICGC DataPortalENSG00000264857
TCGA cBioPortalMIR5696
AceView (NCBI)MIR5696
Genatlas (Paris)MIR5696
WikiGenes100847007
SOURCE (Princeton)MIR5696
Genetics Home Reference (NIH)MIR5696
miRBaseMIR5696
dbDEMCMIR5696
Genomic and cartography
GoldenPath hg19 (UCSC)MIR5696  -     chr2:101925912-101925996 +  2q11.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR5696  -     2q11.2   [Description]    (hg38-Dec_2013)
EnsemblMIR5696 - 2q11.2 [CytoView hg19]  MIR5696 - 2q11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR5696 [Mapview hg19]  MIR5696 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000002 NC_018913 NT_005403 NW_004929303
Consensus coding sequences : CCDS (NCBI)MIR5696
Alternative Splicing GalleryENSG00000264857
Gene ExpressionMIR5696 [ NCBI-GEO ]   MIR5696 [ EBI - ARRAY_EXPRESS ]   MIR5696 [ SEEK ]   MIR5696 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5696 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847007
GTEX Portal (Tissue expression)MIR5696
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5696
DMDM Disease mutations100847007
Blocks (Seattle)MIR5696
Human Protein AtlasENSG00000264857
Protein Interaction databases
FunCoupENSG00000264857
BioGRIDMIR5696
STRING (EMBL)MIR5696
ZODIACMIR5696
Ontologies - Pathways
Huge Navigator MIR5696 [HugePedia]
snp3D : Map Gene to Disease100847007
BioCentury BCIQMIR5696
ClinGenMIR5696
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847007
Clinical trialMIR5696
Miscellaneous
canSAR (ICR)MIR5696 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5696
EVEXMIR5696
GoPubMedMIR5696
iHOPMIR5696
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 Mar 14 12:31:45 CET 2017

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