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MIR4689 (microRNA 4689)

Identity

Alias_symbol (synonym)hsa-mir-4689
Other aliasmir-4689
HGNC (Hugo) MIR4689
LocusID (NCBI) 100616421
Atlas_Id 69604
Location 1p36.31  [Link to chromosome band 1p36]
Location_base_pair Starts at 5922732 and ends at 5922801 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)MIR4689   41895
Cards
Entrez_Gene (NCBI)MIR4689  100616421  microRNA 4689
Aliasesmir-4689
GeneCards (Weizmann)MIR4689
Ensembl hg19 (Hinxton)ENSG00000264101 [Gene_View]  chr1:5922732-5922801 [Contig_View]  MIR4689 [Vega]
Ensembl hg38 (Hinxton)ENSG00000264101 [Gene_View]  chr1:5922732-5922801 [Contig_View]  MIR4689 [Vega]
ICGC DataPortalENSG00000264101
TCGA cBioPortalMIR4689
AceView (NCBI)MIR4689
Genatlas (Paris)MIR4689
WikiGenes100616421
SOURCE (Princeton)MIR4689
Genetics Home Reference (NIH)MIR4689
miRBaseMIR4689
dbDEMCMIR4689
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4689  -     chr1:5922732-5922801 -  1p36.31   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4689  -     1p36.31   [Description]    (hg38-Dec_2013)
EnsemblMIR4689 - 1p36.31 [CytoView hg19]  MIR4689 - 1p36.31 [CytoView hg38]
Mapping of homologs : NCBIMIR4689 [Mapview hg19]  MIR4689 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611382
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929289
Consensus coding sequences : CCDS (NCBI)MIR4689
Alternative Splicing GalleryENSG00000264101
Gene ExpressionMIR4689 [ NCBI-GEO ]   MIR4689 [ EBI - ARRAY_EXPRESS ]   MIR4689 [ SEEK ]   MIR4689 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4689 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616421
GTEX Portal (Tissue expression)MIR4689
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4689
DMDM Disease mutations100616421
Blocks (Seattle)MIR4689
Human Protein AtlasENSG00000264101
Protein Interaction databases
FunCoupENSG00000264101
BioGRIDMIR4689
STRING (EMBL)MIR4689
ZODIACMIR4689
Ontologies - Pathways
Huge Navigator MIR4689 [HugePedia]
snp3D : Map Gene to Disease100616421
BioCentury BCIQMIR4689
ClinGenMIR4689
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616421
Clinical trialMIR4689
Miscellaneous
canSAR (ICR)MIR4689 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4689
EVEXMIR4689
GoPubMedMIR4689
iHOPMIR4689
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 12:30:45 CET 2017

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