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MIR4779 (microRNA 4779)

Identity

Alias_symbol (synonym)hsa-mir-4779
Other alias-
HGNC (Hugo) MIR4779
LocusID (NCBI) 100616159
Atlas_Id 78504
Location 2p11.2  [Link to chromosome band 2p11]
Location_base_pair Starts at 86420149 and ends at 86420231 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)MIR4779   41747
Cards
Entrez_Gene (NCBI)MIR4779  100616159  microRNA 4779
Aliases
GeneCards (Weizmann)MIR4779
Ensembl hg19 (Hinxton)ENSG00000265420 [Gene_View]  chr2:86420149-86420231 [Contig_View]  MIR4779 [Vega]
Ensembl hg38 (Hinxton)ENSG00000265420 [Gene_View]  chr2:86420149-86420231 [Contig_View]  MIR4779 [Vega]
ICGC DataPortalENSG00000265420
TCGA cBioPortalMIR4779
AceView (NCBI)MIR4779
Genatlas (Paris)MIR4779
WikiGenes100616159
SOURCE (Princeton)MIR4779
Genetics Home Reference (NIH)MIR4779
miRBaseMIR4779
dbDEMCMIR4779
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4779  -     chr2:86420149-86420231 -  2p11.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4779  -     2p11.2   [Description]    (hg38-Dec_2013)
EnsemblMIR4779 - 2p11.2 [CytoView hg19]  MIR4779 - 2p11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4779 [Mapview hg19]  MIR4779 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4779
Alternative Splicing GalleryENSG00000265420
Gene ExpressionMIR4779 [ NCBI-GEO ]   MIR4779 [ EBI - ARRAY_EXPRESS ]   MIR4779 [ SEEK ]   MIR4779 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4779 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616159
GTEX Portal (Tissue expression)MIR4779
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4779
DMDM Disease mutations100616159
Blocks (Seattle)MIR4779
Human Protein AtlasENSG00000265420
Protein Interaction databases
FunCoupENSG00000265420
BioGRIDMIR4779
STRING (EMBL)MIR4779
ZODIACMIR4779
Ontologies - Pathways
Huge Navigator MIR4779 [HugePedia]
snp3D : Map Gene to Disease100616159
BioCentury BCIQMIR4779
ClinGenMIR4779
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616159
Clinical trialMIR4779
Miscellaneous
canSAR (ICR)MIR4779 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4779
EVEXMIR4779
GoPubMedMIR4779
iHOPMIR4779
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 12:31:04 CET 2017

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