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MIR4756 (microRNA 4756)

Identity

Alias_symbol (synonym)hsa-mir-4756
Other alias-
HGNC (Hugo) MIR4756
LocusID (NCBI) 100616225
Atlas_Id 69669
Location 20q13.2  [Link to chromosome band 20q13]
Location_base_pair Starts at 54068408 and ends at 54068485 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)MIR4756   41529
Cards
Entrez_Gene (NCBI)MIR4756  100616225  microRNA 4756
Aliases
GeneCards (Weizmann)MIR4756
Ensembl hg19 (Hinxton)ENSG00000265595 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265595 [Gene_View]  chr20:54068408-54068485 [Contig_View]  MIR4756 [Vega]
ICGC DataPortalENSG00000265595
TCGA cBioPortalMIR4756
AceView (NCBI)MIR4756
Genatlas (Paris)MIR4756
WikiGenes100616225
SOURCE (Princeton)MIR4756
Genetics Home Reference (NIH)MIR4756
miRBaseMIR4756
dbDEMCMIR4756
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4756  -     chr20:54068408-54068485 -  20q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4756  -     20q13.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4756 - 20q13.2 [CytoView hg19]  MIR4756 - 20q13.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4756 [Mapview hg19]  MIR4756 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4756
Alternative Splicing GalleryENSG00000265595
Gene ExpressionMIR4756 [ NCBI-GEO ]   MIR4756 [ EBI - ARRAY_EXPRESS ]   MIR4756 [ SEEK ]   MIR4756 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4756 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616225
GTEX Portal (Tissue expression)MIR4756
Human Protein AtlasENSG00000265595-MIR4756 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4756
DMDM Disease mutations100616225
Blocks (Seattle)MIR4756
Human Protein Atlas [tissue]ENSG00000265595-MIR4756 [tissue]
Protein Interaction databases
FunCoupENSG00000265595
BioGRIDMIR4756
STRING (EMBL)MIR4756
ZODIACMIR4756
Ontologies - Pathways
Huge Navigator MIR4756 [HugePedia]
snp3D : Map Gene to Disease100616225
BioCentury BCIQMIR4756
ClinGenMIR4756
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616225
Clinical trialMIR4756
Miscellaneous
canSAR (ICR)MIR4756 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4756
EVEXMIR4756
GoPubMedMIR4756
iHOPMIR4756
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:41:55 CET 2017

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