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MIR5694 (microRNA 5694)

Identity

Alias_symbol (synonym)hsa-mir-5694
Other alias-
HGNC (Hugo) MIR5694
LocusID (NCBI) 100847064
Atlas_Id 69890
Location 10q26.12  [Link to chromosome band 10q26]
Location_base_pair Starts at 122344591 and ends at 122806858 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)MIR5694   43530
Cards
Entrez_Gene (NCBI)MIR5694  100847064  microRNA 5694
Aliases
GeneCards (Weizmann)MIR5694
Ensembl hg19 (Hinxton)ENSG00000265993 [Gene_View]  chr10:122344591-122806858 [Contig_View]  MIR5694 [Vega]
Ensembl hg38 (Hinxton)ENSG00000265993 [Gene_View]  chr10:122344591-122806858 [Contig_View]  MIR5694 [Vega]
ICGC DataPortalENSG00000265993
TCGA cBioPortalMIR5694
AceView (NCBI)MIR5694
Genatlas (Paris)MIR5694
WikiGenes100847064
SOURCE (Princeton)MIR5694
Genetics Home Reference (NIH)MIR5694
miRBaseMIR5694
dbDEMCMIR5694
Genomic and cartography
GoldenPath hg19 (UCSC)MIR5694  -     chr10:122344591-122806858 +  10q26.12   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR5694  -     10q26.12   [Description]    (hg38-Dec_2013)
EnsemblMIR5694 - 10q26.12 [CytoView hg19]  MIR5694 - 10q26.12 [CytoView hg38]
Mapping of homologs : NCBIMIR5694 [Mapview hg19]  MIR5694 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)MIR5694
Alternative Splicing GalleryENSG00000265993
Gene ExpressionMIR5694 [ NCBI-GEO ]   MIR5694 [ EBI - ARRAY_EXPRESS ]   MIR5694 [ SEEK ]   MIR5694 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5694 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847064
GTEX Portal (Tissue expression)MIR5694
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5694
DMDM Disease mutations100847064
Blocks (Seattle)MIR5694
Human Protein AtlasENSG00000265993
Protein Interaction databases
FunCoupENSG00000265993
BioGRIDMIR5694
STRING (EMBL)MIR5694
ZODIACMIR5694
Ontologies - Pathways
Huge Navigator MIR5694 [HugePedia]
snp3D : Map Gene to Disease100847064
BioCentury BCIQMIR5694
ClinGenMIR5694
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847064
Clinical trialMIR5694
Miscellaneous
canSAR (ICR)MIR5694 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5694
EVEXMIR5694
GoPubMedMIR5694
iHOPMIR5694
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:31:45 CET 2017

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