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MIR4786 (microRNA 4786)

Identity

Alias_symbol (synonym)hsa-mir-4786
Other aliasmir-4786
HGNC (Hugo) MIR4786
LocusID (NCBI) 100616417
Atlas_Id 69700
Location 2q37.3  [Link to chromosome band 2q37]
Location_base_pair Starts at 239943015 and ends at 239943094 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)MIR4786   41751
Cards
Entrez_Gene (NCBI)MIR4786  100616417  microRNA 4786
Aliasesmir-4786
GeneCards (Weizmann)MIR4786
Ensembl hg19 (Hinxton)ENSG00000264279 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264279 [Gene_View]  chr2:239943015-239943094 [Contig_View]  MIR4786 [Vega]
ICGC DataPortalENSG00000264279
TCGA cBioPortalMIR4786
AceView (NCBI)MIR4786
Genatlas (Paris)MIR4786
WikiGenes100616417
SOURCE (Princeton)MIR4786
Genetics Home Reference (NIH)MIR4786
miRBaseMIR4786
dbDEMCMIR4786
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4786  -     chr2:239943015-239943094 -  2q37.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4786  -     2q37.3   [Description]    (hg19-Feb_2009)
EnsemblMIR4786 - 2q37.3 [CytoView hg19]  MIR4786 - 2q37.3 [CytoView hg38]
Mapping of homologs : NCBIMIR4786 [Mapview hg19]  MIR4786 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611421
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4786
Alternative Splicing GalleryENSG00000264279
Gene ExpressionMIR4786 [ NCBI-GEO ]   MIR4786 [ EBI - ARRAY_EXPRESS ]   MIR4786 [ SEEK ]   MIR4786 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4786 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616417
GTEX Portal (Tissue expression)MIR4786
Human Protein AtlasENSG00000264279-MIR4786 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4786
DMDM Disease mutations100616417
Blocks (Seattle)MIR4786
Human Protein Atlas [tissue]ENSG00000264279-MIR4786 [tissue]
Protein Interaction databases
FunCoupENSG00000264279
BioGRIDMIR4786
STRING (EMBL)MIR4786
ZODIACMIR4786
Ontologies - Pathways
Huge Navigator MIR4786 [HugePedia]
snp3D : Map Gene to Disease100616417
BioCentury BCIQMIR4786
ClinGenMIR4786
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616417
Clinical trialMIR4786
Miscellaneous
canSAR (ICR)MIR4786 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4786
EVEXseạch9MIR4786 TARGET=EVEX>MIR4786
GoPubMedMIR4786
iHOPMIR4786
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 : Thu Nov 9 12:15:22 CET 2017

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