Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

MIR4739 (microRNA 4739)

Identity

Alias_symbol (synonym)hsa-mir-4739
Other aliasmir-4739
HGNC (Hugo) MIR4739
LocusID (NCBI) 100616170
Atlas_Id 69652
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 77680985 and ends at 77681058 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)MIR4739   41801
Cards
Entrez_Gene (NCBI)MIR4739  100616170  microRNA 4739
Aliasesmir-4739
GeneCards (Weizmann)MIR4739
Ensembl hg19 (Hinxton)ENSG00000266665 [Gene_View]  chr17:77680985-77681058 [Contig_View]  MIR4739 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266665 [Gene_View]  chr17:77680985-77681058 [Contig_View]  MIR4739 [Vega]
ICGC DataPortalENSG00000266665
TCGA cBioPortalMIR4739
AceView (NCBI)MIR4739
Genatlas (Paris)MIR4739
WikiGenes100616170
SOURCE (Princeton)MIR4739
Genetics Home Reference (NIH)MIR4739
miRBaseMIR4739
dbDEMCMIR4739
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4739  -     chr17:77680985-77681058 -  17q25.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4739  -     17q25.3   [Description]    (hg38-Dec_2013)
EnsemblMIR4739 - 17q25.3 [CytoView hg19]  MIR4739 - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4739 [Mapview hg19]  MIR4739 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611400
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010783 NW_004929407
Consensus coding sequences : CCDS (NCBI)MIR4739
Alternative Splicing GalleryENSG00000266665
Gene ExpressionMIR4739 [ NCBI-GEO ]   MIR4739 [ EBI - ARRAY_EXPRESS ]   MIR4739 [ SEEK ]   MIR4739 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4739 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616170
GTEX Portal (Tissue expression)MIR4739
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4739
DMDM Disease mutations100616170
Blocks (Seattle)MIR4739
Human Protein AtlasENSG00000266665
Protein Interaction databases
FunCoupENSG00000266665
BioGRIDMIR4739
STRING (EMBL)MIR4739
ZODIACMIR4739
Ontologies - Pathways
Huge Navigator MIR4739 [HugePedia]
snp3D : Map Gene to Disease100616170
BioCentury BCIQMIR4739
ClinGenMIR4739
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616170
Clinical trialMIR4739
Miscellaneous
canSAR (ICR)MIR4739 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4739
EVEXMIR4739
GoPubMedMIR4739
iHOPMIR4739
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 12:30:55 CET 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.