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MIR4763 (microRNA 4763)

Identity

Alias_symbol (synonym)hsa-mir-4763
Other alias-
HGNC (Hugo) MIR4763
LocusID (NCBI) 100616143
Atlas_Id 69676
Location 22q13.31  [Link to chromosome band 22q13]
Location_base_pair Starts at 46113566 and ends at 46113657 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)MIR4763   41677
Cards
Entrez_Gene (NCBI)MIR4763  100616143  microRNA 4763
Aliases
GeneCards (Weizmann)MIR4763
Ensembl hg19 (Hinxton)ENSG00000264147 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264147 [Gene_View]  chr22:46113566-46113657 [Contig_View]  MIR4763 [Vega]
ICGC DataPortalENSG00000264147
TCGA cBioPortalMIR4763
AceView (NCBI)MIR4763
Genatlas (Paris)MIR4763
WikiGenes100616143
SOURCE (Princeton)MIR4763
Genetics Home Reference (NIH)MIR4763
miRBaseMIR4763
dbDEMCMIR4763
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4763  -     chr22:46113566-46113657 +  22q13.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4763  -     22q13.31   [Description]    (hg19-Feb_2009)
EnsemblMIR4763 - 22q13.31 [CytoView hg19]  MIR4763 - 22q13.31 [CytoView hg38]
Mapping of homologs : NCBIMIR4763 [Mapview hg19]  MIR4763 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4763
Alternative Splicing GalleryENSG00000264147
Gene ExpressionMIR4763 [ NCBI-GEO ]   MIR4763 [ EBI - ARRAY_EXPRESS ]   MIR4763 [ SEEK ]   MIR4763 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4763 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616143
GTEX Portal (Tissue expression)MIR4763
Human Protein AtlasENSG00000264147-MIR4763 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4763
DMDM Disease mutations100616143
Blocks (Seattle)MIR4763
Human Protein Atlas [tissue]ENSG00000264147-MIR4763 [tissue]
Protein Interaction databases
FunCoupENSG00000264147
BioGRIDMIR4763
STRING (EMBL)MIR4763
ZODIACMIR4763
Ontologies - Pathways
Huge Navigator MIR4763 [HugePedia]
snp3D : Map Gene to Disease100616143
BioCentury BCIQMIR4763
ClinGenMIR4763
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616143
Clinical trialMIR4763
Miscellaneous
canSAR (ICR)MIR4763 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4763
EVEXMIR4763
GoPubMedMIR4763
iHOPMIR4763
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 13:44:00 CET 2017

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