Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR941-5 (microRNA 941-5)

Identity

Other alias-
HGNC (Hugo) MIR941-5
LocusID (NCBI) 103504732
Atlas_Id 76763
Location 20q13.33  [Link to chromosome band 20q13]
Location_base_pair Starts at 63919561 and ends at 63919632 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)MIR941-5   50845
Cards
Entrez_Gene (NCBI)MIR941-5  103504732  microRNA 941-5
Aliases
GeneCards (Weizmann)MIR941-5
Ensembl hg19 (Hinxton)ENSG00000275842 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275842 [Gene_View]  chr20:63919561-63919632 [Contig_View]  MIR941-5 [Vega]
ICGC DataPortalENSG00000275842
TCGA cBioPortalMIR941-5
AceView (NCBI)MIR941-5
Genatlas (Paris)MIR941-5
WikiGenes103504732
SOURCE (Princeton)MIR941-5
Genetics Home Reference (NIH)MIR941-5
miRBaseMIR941-5
dbDEMCMIR941-5
Genomic and cartography
GoldenPath hg38 (UCSC)MIR941-5  -     chr20:63919561-63919632 +  20q13.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR941-5  -     20q13.33   [Description]    (hg19-Feb_2009)
EnsemblMIR941-5 - 20q13.33 [CytoView hg19]  MIR941-5 - 20q13.33 [CytoView hg38]
Mapping of homologs : NCBIMIR941-5 [Mapview hg19]  MIR941-5 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611895
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR941-5
Alternative Splicing GalleryENSG00000275842
Gene ExpressionMIR941-5 [ NCBI-GEO ]   MIR941-5 [ EBI - ARRAY_EXPRESS ]   MIR941-5 [ SEEK ]   MIR941-5 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR941-5 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)103504732
GTEX Portal (Tissue expression)MIR941-5
Human Protein AtlasENSG00000275842-MIR941-5 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR941-5
DMDM Disease mutations103504732
Blocks (Seattle)MIR941-5
Human Protein Atlas [tissue]ENSG00000275842-MIR941-5 [tissue]
Protein Interaction databases
FunCoupENSG00000275842
BioGRIDMIR941-5
STRING (EMBL)MIR941-5
ZODIACMIR941-5
Ontologies - Pathways
Huge Navigator MIR941-5 [HugePedia]
snp3D : Map Gene to Disease103504732
BioCentury BCIQMIR941-5
ClinGenMIR941-5
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD103504732
Clinical trialMIR941-5
Miscellaneous
canSAR (ICR)MIR941-5 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR941-5
EVEXMIR941-5
GoPubMedMIR941-5
iHOPMIR941-5
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 Nov 21 13:41:59 CET 2017

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