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MIR4719 (microRNA 4719)

Identity

Alias_symbol (synonym)hsa-mir-4719
Other alias-
HGNC (Hugo) MIR4719
LocusID (NCBI) 100616172
Atlas_Id 69633
Location 16q23.1  [Link to chromosome band 16q23]
Location_base_pair Starts at 76868936 and ends at 76869019 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)MIR4719   41807
Cards
Entrez_Gene (NCBI)MIR4719  100616172  microRNA 4719
Aliases
GeneCards (Weizmann)MIR4719
Ensembl hg19 (Hinxton)ENSG00000266426 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266426 [Gene_View]  chr16:76868936-76869019 [Contig_View]  MIR4719 [Vega]
ICGC DataPortalENSG00000266426
TCGA cBioPortalMIR4719
AceView (NCBI)MIR4719
Genatlas (Paris)MIR4719
WikiGenes100616172
SOURCE (Princeton)MIR4719
Genetics Home Reference (NIH)MIR4719
miRBaseMIR4719
dbDEMCMIR4719
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4719  -     chr16:76868936-76869019 +  16q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4719  -     16q23.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4719 - 16q23.1 [CytoView hg19]  MIR4719 - 16q23.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4719 [Mapview hg19]  MIR4719 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4719
Alternative Splicing GalleryENSG00000266426
Gene ExpressionMIR4719 [ NCBI-GEO ]   MIR4719 [ EBI - ARRAY_EXPRESS ]   MIR4719 [ SEEK ]   MIR4719 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4719 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616172
GTEX Portal (Tissue expression)MIR4719
Human Protein AtlasENSG00000266426-MIR4719 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4719
DMDM Disease mutations100616172
Blocks (Seattle)MIR4719
Human Protein Atlas [tissue]ENSG00000266426-MIR4719 [tissue]
Protein Interaction databases
FunCoupENSG00000266426
BioGRIDMIR4719
STRING (EMBL)MIR4719
ZODIACMIR4719
Ontologies - Pathways
Huge Navigator MIR4719 [HugePedia]
snp3D : Map Gene to Disease100616172
BioCentury BCIQMIR4719
ClinGenMIR4719
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616172
Clinical trialMIR4719
Miscellaneous
canSAR (ICR)MIR4719 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4719
EVEXMIR4719
GoPubMedMIR4719
iHOPMIR4719
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 : Thu Nov 9 12:15:08 CET 2017

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