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MIR4289 (microRNA 4289)

Identity

Alias_symbol (synonym)hsa-mir-4289
Other alias-
HGNC (Hugo) MIR4289
LocusID (NCBI) 100423015
Atlas_Id 69395
Location 9q22.1  [Link to chromosome band 9q22]
Location_base_pair Starts at 88745836 and ends at 88745905 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)MIR4289   38278
Cards
Entrez_Gene (NCBI)MIR4289  100423015  microRNA 4289
Aliases
GeneCards (Weizmann)MIR4289
Ensembl hg19 (Hinxton)ENSG00000265873 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265873 [Gene_View]  chr9:88745836-88745905 [Contig_View]  MIR4289 [Vega]
ICGC DataPortalENSG00000265873
TCGA cBioPortalMIR4289
AceView (NCBI)MIR4289
Genatlas (Paris)MIR4289
WikiGenes100423015
SOURCE (Princeton)MIR4289
Genetics Home Reference (NIH)MIR4289
miRBaseMIR4289
dbDEMCMIR4289
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4289  -     chr9:88745836-88745905 -  9q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4289  -     9q22.1   [Description]    (hg19-Feb_2009)
EnsemblMIR4289 - 9q22.1 [CytoView hg19]  MIR4289 - 9q22.1 [CytoView hg38]
Mapping of homologs : NCBIMIR4289 [Mapview hg19]  MIR4289 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4289
Alternative Splicing GalleryENSG00000265873
Gene ExpressionMIR4289 [ NCBI-GEO ]   MIR4289 [ EBI - ARRAY_EXPRESS ]   MIR4289 [ SEEK ]   MIR4289 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4289 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100423015
GTEX Portal (Tissue expression)MIR4289
Human Protein AtlasENSG00000265873-MIR4289 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4289
DMDM Disease mutations100423015
Blocks (Seattle)MIR4289
Human Protein Atlas [tissue]ENSG00000265873-MIR4289 [tissue]
Protein Interaction databases
FunCoupENSG00000265873
BioGRIDMIR4289
STRING (EMBL)MIR4289
ZODIACMIR4289
Ontologies - Pathways
Huge Navigator MIR4289 [HugePedia]
snp3D : Map Gene to Disease100423015
BioCentury BCIQMIR4289
ClinGenMIR4289
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100423015
Chemical/Pharm GKB GenePA165585859
Clinical trialMIR4289
Miscellaneous
canSAR (ICR)MIR4289 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4289
EVEXMIR4289
GoPubMedMIR4289
iHOPMIR4289
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 12:14:14 CET 2017

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