Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR5092 (microRNA 5092)

Identity

Alias_symbol (synonym)hsa-mir-5092
Other alias-
HGNC (Hugo) MIR5092
LocusID (NCBI) 100847039
Atlas_Id 69746
Location 3q21.2  [Link to chromosome band 3q21]
Location_base_pair Starts at 125151465 and ends at 125151552 bp from pter ( according to hg38-Dec_2013)

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)MIR5092   43467
Cards
Entrez_Gene (NCBI)MIR5092  100847039  microRNA 5092
Aliases
GeneCards (Weizmann)MIR5092
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr3:125151465-125151552 [Contig_View]  MIR5092 [Vega]
TCGA cBioPortalMIR5092
AceView (NCBI)MIR5092
Genatlas (Paris)MIR5092
WikiGenes100847039
SOURCE (Princeton)MIR5092
Genetics Home Reference (NIH)MIR5092
miRBaseMIR5092
dbDEMCMIR5092
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5092  -     chr3:125151465-125151552 -  3q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5092  -     3q21.2   [Description]    (hg19-Feb_2009)
EnsemblMIR5092 - 3q21.2 [CytoView hg19]  MIR5092 - 3q21.2 [CytoView hg38]
Mapping of homologs : NCBIMIR5092 [Mapview hg19]  MIR5092 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5092
Gene ExpressionMIR5092 [ NCBI-GEO ]   MIR5092 [ EBI - ARRAY_EXPRESS ]   MIR5092 [ SEEK ]   MIR5092 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5092 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847039
GTEX Portal (Tissue expression)MIR5092
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5092
DMDM Disease mutations100847039
Blocks (Seattle)MIR5092
Protein Interaction databases
BioGRIDMIR5092
STRING (EMBL)MIR5092
ZODIACMIR5092
Ontologies - Pathways
Huge Navigator MIR5092 [HugePedia]
snp3D : Map Gene to Disease100847039
BioCentury BCIQMIR5092
ClinGenMIR5092
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847039
Clinical trialMIR5092
Miscellaneous
canSAR (ICR)MIR5092 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5092
EVEXMIR5092
GoPubMedMIR5092
iHOPMIR5092
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 : Mon Sep 18 13:29:28 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.