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MIR6089 (microRNA 6089)

Identity

Alias_namesMIR6089-1
MIR6089-2
microRNA 6089-1
microRNA 6089-2
Alias_symbol (synonym)hsa-mir-6089-1
Other aliashsa-mir-6089-2
HGNC (Hugo) MIR6089
LocusID (NCBI) 102464837
Atlas_Id 69940
Location Xp22.33  [Link to chromosome band Xp22]
Location_base_pair Starts at 2609191 and ends at 2609254 bp from pter ( according to hg38-Dec_2013)

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)MIR6089   50179
Cards
Entrez_Gene (NCBI)MIR6089  102464837  microRNA 6089
AliasesMIR6089-1; MIR6089-2; hsa-mir-6089-1; hsa-mir-6089-2
GeneCards (Weizmann)MIR6089
Ensembl hg19 (Hinxton)ENSG00000277120 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277120 [Gene_View]  chrX:2609191-2609254 [Contig_View]  MIR6089 [Vega]
ICGC DataPortalENSG00000277120
TCGA cBioPortalMIR6089
AceView (NCBI)MIR6089
Genatlas (Paris)MIR6089
WikiGenes102464837
SOURCE (Princeton)MIR6089
Genetics Home Reference (NIH)MIR6089
miRBaseMIR6089
dbDEMCMIR6089
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6089  -     chrX:2609191-2609254 +  Xp22.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6089  -     Xp22.33   [Description]    (hg19-Feb_2009)
EnsemblMIR6089 - Xp22.33 [CytoView hg19]  MIR6089 - Xp22.33 [CytoView hg38]
Mapping of homologs : NCBIMIR6089 [Mapview hg19]  MIR6089 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR6089
Alternative Splicing GalleryENSG00000277120
Gene ExpressionMIR6089 [ NCBI-GEO ]   MIR6089 [ EBI - ARRAY_EXPRESS ]   MIR6089 [ SEEK ]   MIR6089 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6089 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102464837
GTEX Portal (Tissue expression)MIR6089
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6089
DMDM Disease mutations102464837
Blocks (Seattle)MIR6089
Human Protein AtlasENSG00000277120
Protein Interaction databases
FunCoupENSG00000277120
BioGRIDMIR6089
STRING (EMBL)MIR6089
ZODIACMIR6089
Ontologies - Pathways
Huge Navigator MIR6089 [HugePedia]
snp3D : Map Gene to Disease102464837
BioCentury BCIQMIR6089
ClinGenMIR6089
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102464837
Clinical trialMIR6089
Miscellaneous
canSAR (ICR)MIR6089 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6089
EVEXMIR6089
GoPubMedMIR6089
iHOPMIR6089
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 : Wed May 31 15:29:45 CEST 2017

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