Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR4639 (microRNA 4639)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR4639
HGNC Alias symbhsa-mir-4639
LocusID (NCBI) 100616269
Atlas_Id 69552
Location 6p22.3  [Link to chromosome band 6p22]
Location_base_pair Starts at 16141556 and ends at 16141624 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)MIR4639   41645
Cards
Entrez_Gene (NCBI)MIR4639  100616269  microRNA 4639
Aliases
GeneCards (Weizmann)MIR4639
Ensembl hg19 (Hinxton)ENSG00000263712 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263712 [Gene_View]  ENSG00000263712 [Sequence]  chr6:16141556-16141624 [Contig_View]  MIR4639 [Vega]
ICGC DataPortalENSG00000263712
TCGA cBioPortalMIR4639
AceView (NCBI)MIR4639
Genatlas (Paris)MIR4639
WikiGenes100616269
SOURCE (Princeton)MIR4639
Genetics Home Reference (NIH)MIR4639
miRBaseMIR4639
dbDEMCMIR4639
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4639  -     chr6:16141556-16141624 +  6p22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4639  -     6p22.3   [Description]    (hg19-Feb_2009)
GoldenPathMIR4639 - 6p22.3 [CytoView hg19]  MIR4639 - 6p22.3 [CytoView hg38]
ImmunoBaseENSG00000263712
genome Data Viewer NCBIMIR4639 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4639
Alternative Splicing GalleryENSG00000263712
Gene ExpressionMIR4639 [ NCBI-GEO ]   MIR4639 [ EBI - ARRAY_EXPRESS ]   MIR4639 [ SEEK ]   MIR4639 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4639 [ Firebrowse - Broad ]
GenevisibleExpression of MIR4639 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100616269
GTEX Portal (Tissue expression)MIR4639
Human Protein AtlasENSG00000263712-MIR4639 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4639
DMDM Disease mutations100616269
Blocks (Seattle)MIR4639
Human Protein Atlas [tissue]ENSG00000263712-MIR4639 [tissue]
Protein Interaction databases
FunCoupENSG00000263712
BioGRIDMIR4639
STRING (EMBL)MIR4639
ZODIACMIR4639
Ontologies - Pathways
Huge Navigator MIR4639 [HugePedia]
snp3D : Map Gene to Disease100616269
BioCentury BCIQMIR4639
ClinGenMIR4639
Clinical trials, drugs, therapy
Protein Interactions : CTD100616269
Clinical trialMIR4639
Miscellaneous
canSAR (ICR)MIR4639 (select the gene name)
HarmonizomeMIR4639
DataMed IndexMIR4639
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4639
EVEXMIR4639
GoPubMedMIR4639
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Sat Aug 22 19:26:05 CEST 2020

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