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MIR5693 (microRNA 5693)

Identity

Alias_symbol (synonym)hsa-mir-5693
Other alias-
HGNC (Hugo) MIR5693
LocusID (NCBI) 100847003
Atlas_Id 69889
Location 13q14.3  [Link to chromosome band 13q14]
Location_base_pair Starts at 51922703 and ends at 51922775 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)MIR5693   43499
Cards
Entrez_Gene (NCBI)MIR5693  100847003  microRNA 5693
Aliases
GeneCards (Weizmann)MIR5693
Ensembl hg19 (Hinxton)ENSG00000266072 [Gene_View]  chr13:51922703-51922775 [Contig_View]  MIR5693 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266072 [Gene_View]  chr13:51922703-51922775 [Contig_View]  MIR5693 [Vega]
ICGC DataPortalENSG00000266072
TCGA cBioPortalMIR5693
AceView (NCBI)MIR5693
Genatlas (Paris)MIR5693
WikiGenes100847003
SOURCE (Princeton)MIR5693
Genetics Home Reference (NIH)MIR5693
miRBaseMIR5693
dbDEMCMIR5693
Genomic and cartography
GoldenPath hg19 (UCSC)MIR5693  -     chr13:51922703-51922775 -  13q14.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR5693  -     13q14.3   [Description]    (hg38-Dec_2013)
EnsemblMIR5693 - 13q14.3 [CytoView hg19]  MIR5693 - 13q14.3 [CytoView hg38]
Mapping of homologs : NCBIMIR5693 [Mapview hg19]  MIR5693 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000013 NC_018924 NT_024524 NW_004929388
Consensus coding sequences : CCDS (NCBI)MIR5693
Alternative Splicing GalleryENSG00000266072
Gene ExpressionMIR5693 [ NCBI-GEO ]   MIR5693 [ EBI - ARRAY_EXPRESS ]   MIR5693 [ SEEK ]   MIR5693 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5693 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847003
GTEX Portal (Tissue expression)MIR5693
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5693
DMDM Disease mutations100847003
Blocks (Seattle)MIR5693
Human Protein AtlasENSG00000266072
Protein Interaction databases
FunCoupENSG00000266072
BioGRIDMIR5693
STRING (EMBL)MIR5693
ZODIACMIR5693
Ontologies - Pathways
Huge Navigator MIR5693 [HugePedia]
snp3D : Map Gene to Disease100847003
BioCentury BCIQMIR5693
ClinGenMIR5693
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847003
Clinical trialMIR5693
Miscellaneous
canSAR (ICR)MIR5693 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5693
EVEXMIR5693
GoPubMedMIR5693
iHOPMIR5693
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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