Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR1913 (microRNA 1913)

Identity

Alias (NCBI)MIRN1913
hsa-mir-1913
HGNC (Hugo) MIR1913
HGNC Alias symbhsa-mir-1913
HGNC Previous nameMIRN1913
LocusID (NCBI) 100302141
Atlas_Id 69096
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 166509354 and ends at 166509433 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)MIR1913   35397
Cards
Entrez_Gene (NCBI)MIR1913  100302141  microRNA 1913
AliasesMIRN1913; hsa-mir-1913
GeneCards (Weizmann)MIR1913
Ensembl hg19 (Hinxton)ENSG00000222958 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000222958 [Gene_View]  ENSG00000222958 [Sequence]  chr6:166509354-166509433 [Contig_View]  MIR1913 [Vega]
ICGC DataPortalENSG00000222958
TCGA cBioPortalMIR1913
AceView (NCBI)MIR1913
Genatlas (Paris)MIR1913
WikiGenes100302141
SOURCE (Princeton)MIR1913
Genetics Home Reference (NIH)MIR1913
miRBaseMIR1913
dbDEMCMIR1913
Genomic and cartography
GoldenPath hg38 (UCSC)MIR1913  -     chr6:166509354-166509433 -  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR1913  -     6q27   [Description]    (hg19-Feb_2009)
GoldenPathMIR1913 - 6q27 [CytoView hg19]  MIR1913 - 6q27 [CytoView hg38]
ImmunoBaseENSG00000222958
genome Data Viewer NCBIMIR1913 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR1913
Alternative Splicing GalleryENSG00000222958
Gene ExpressionMIR1913 [ NCBI-GEO ]   MIR1913 [ EBI - ARRAY_EXPRESS ]   MIR1913 [ SEEK ]   MIR1913 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR1913 [ Firebrowse - Broad ]
GenevisibleExpression of MIR1913 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100302141
GTEX Portal (Tissue expression)MIR1913
Human Protein AtlasENSG00000222958-MIR1913 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR1913
DMDM Disease mutations100302141
Blocks (Seattle)MIR1913
Human Protein Atlas [tissue]ENSG00000222958-MIR1913 [tissue]
Protein Interaction databases
FunCoupENSG00000222958
BioGRIDMIR1913
STRING (EMBL)MIR1913
ZODIACMIR1913
Ontologies - Pathways
Huge Navigator MIR1913 [HugePedia]
snp3D : Map Gene to Disease100302141
BioCentury BCIQMIR1913
ClinGenMIR1913
Clinical trials, drugs, therapy
Protein Interactions : CTD100302141
Pharm GKB GenePA164722547
Clinical trialMIR1913
Miscellaneous
canSAR (ICR)MIR1913 (select the gene name)
HarmonizomeMIR1913
DataMed IndexMIR1913
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR1913
EVEXMIR1913
GoPubMedMIR1913
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Aug 22 19:25:01 CEST 2020

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