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

MIR5094 (microRNA 5094)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR5094
HGNC Alias symbhsa-mir-5094
LocusID (NCBI) 100847059
Atlas_Id 69749
Location 15q26.1  [Link to chromosome band 15q26]
Location_base_pair Starts at 89850637 and ends at 89850721 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)MIR5094   43519
Cards
Entrez_Gene (NCBI)MIR5094  100847059  microRNA 5094
Aliases
GeneCards (Weizmann)MIR5094
Ensembl hg19 (Hinxton)ENSG00000264966 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264966 [Gene_View]  ENSG00000264966 [Sequence]  chr15:89850637-89850721 [Contig_View]  MIR5094 [Vega]
ICGC DataPortalENSG00000264966
TCGA cBioPortalMIR5094
AceView (NCBI)MIR5094
Genatlas (Paris)MIR5094
WikiGenes100847059
SOURCE (Princeton)MIR5094
Genetics Home Reference (NIH)MIR5094
miRBaseMIR5094
dbDEMCMIR5094
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5094  -     chr15:89850637-89850721 -  15q26.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5094  -     15q26.1   [Description]    (hg19-Feb_2009)
GoldenPathMIR5094 - 15q26.1 [CytoView hg19]  MIR5094 - 15q26.1 [CytoView hg38]
ImmunoBaseENSG00000264966
genome Data Viewer NCBIMIR5094 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5094
Alternative Splicing GalleryENSG00000264966
Gene ExpressionMIR5094 [ NCBI-GEO ]   MIR5094 [ EBI - ARRAY_EXPRESS ]   MIR5094 [ SEEK ]   MIR5094 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5094 [ Firebrowse - Broad ]
GenevisibleExpression of MIR5094 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100847059
GTEX Portal (Tissue expression)MIR5094
Human Protein AtlasENSG00000264966-MIR5094 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5094
DMDM Disease mutations100847059
Blocks (Seattle)MIR5094
Human Protein Atlas [tissue]ENSG00000264966-MIR5094 [tissue]
Protein Interaction databases
FunCoupENSG00000264966
BioGRIDMIR5094
STRING (EMBL)MIR5094
ZODIACMIR5094
Ontologies - Pathways
Huge Navigator MIR5094 [HugePedia]
snp3D : Map Gene to Disease100847059
BioCentury BCIQMIR5094
ClinGenMIR5094
Clinical trials, drugs, therapy
Protein Interactions : CTD100847059
Clinical trialMIR5094
Miscellaneous
canSAR (ICR)MIR5094 (select the gene name)
HarmonizomeMIR5094
DataMed IndexMIR5094
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5094
EVEXMIR5094
GoPubMedMIR5094
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 Jul 16 16:16:19 CEST 2020

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.