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MIR4759 (microRNA 4759)

Identity

Alias_symbol (synonym)hsa-mir-4759
Other alias-
HGNC (Hugo) MIR4759
LocusID (NCBI) 100616243
Atlas_Id 69672
Location 21q21.3  [Link to chromosome band 21q21]
Location_base_pair Starts at 28326280 and ends at 28326362 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)MIR4759   41575
Cards
Entrez_Gene (NCBI)MIR4759  100616243  microRNA 4759
Aliases
GeneCards (Weizmann)MIR4759
Ensembl hg19 (Hinxton)ENSG00000266133 [Gene_View]  chr21:28326280-28326362 [Contig_View]  MIR4759 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266133 [Gene_View]  chr21:28326280-28326362 [Contig_View]  MIR4759 [Vega]
ICGC DataPortalENSG00000266133
TCGA cBioPortalMIR4759
AceView (NCBI)MIR4759
Genatlas (Paris)MIR4759
WikiGenes100616243
SOURCE (Princeton)MIR4759
Genetics Home Reference (NIH)MIR4759
miRBaseMIR4759
dbDEMCMIR4759
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4759  -     chr21:28326280-28326362 +  21q21.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4759  -     21q21.3   [Description]    (hg38-Dec_2013)
EnsemblMIR4759 - 21q21.3 [CytoView hg19]  MIR4759 - 21q21.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4759 [Mapview hg19]  MIR4759 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000021 NC_018932 NT_011512 NW_004929426
Consensus coding sequences : CCDS (NCBI)MIR4759
Alternative Splicing GalleryENSG00000266133
Gene ExpressionMIR4759 [ NCBI-GEO ]   MIR4759 [ EBI - ARRAY_EXPRESS ]   MIR4759 [ SEEK ]   MIR4759 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4759 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616243
GTEX Portal (Tissue expression)MIR4759
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4759
DMDM Disease mutations100616243
Blocks (Seattle)MIR4759
Human Protein AtlasENSG00000266133
Protein Interaction databases
FunCoupENSG00000266133
BioGRIDMIR4759
STRING (EMBL)MIR4759
ZODIACMIR4759
Ontologies - Pathways
Huge Navigator MIR4759 [HugePedia]
snp3D : Map Gene to Disease100616243
BioCentury BCIQMIR4759
ClinGenMIR4759
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616243
Clinical trialMIR4759
Miscellaneous
canSAR (ICR)MIR4759 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4759
EVEXMIR4759
GoPubMedMIR4759
iHOPMIR4759
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 12:30:59 CET 2017

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