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MIR6133 (microRNA 6133)

Identity

Alias_symbol (synonym)hsa-mir-6133
Other alias
HGNC (Hugo) MIR6133
LocusID (NCBI) 102465139
Atlas_Id 69954
Location 7q33  [Link to chromosome band 7q33]
Location_base_pair Starts at 133290881 and ends at 133290988 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)MIR6133   50007
Cards
Entrez_Gene (NCBI)MIR6133  102465139  microRNA 6133
Aliaseshsa-mir-6133
GeneCards (Weizmann)MIR6133
Ensembl hg19 (Hinxton)ENSG00000276137 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000276137 [Gene_View]  ENSG00000276137 [Sequence]  chr7:133290881-133290988 [Contig_View]  MIR6133 [Vega]
ICGC DataPortalENSG00000276137
TCGA cBioPortalMIR6133
AceView (NCBI)MIR6133
Genatlas (Paris)MIR6133
WikiGenes102465139
SOURCE (Princeton)MIR6133
Genetics Home Reference (NIH)MIR6133
miRBaseMIR6133
dbDEMCMIR6133
Genomic and cartography
GoldenPath hg38 (UCSC)MIR6133  -     chr7:133290881-133290988 +  7q33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR6133  -     7q33   [Description]    (hg19-Feb_2009)
EnsemblMIR6133 - 7q33 [CytoView hg19]  MIR6133 - 7q33 [CytoView hg38]
Mapping of homologs : NCBIMIR6133 [Mapview hg19]  MIR6133 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR6133
Alternative Splicing GalleryENSG00000276137
Gene ExpressionMIR6133 [ NCBI-GEO ]   MIR6133 [ EBI - ARRAY_EXPRESS ]   MIR6133 [ SEEK ]   MIR6133 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR6133 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102465139
GTEX Portal (Tissue expression)MIR6133
Human Protein AtlasENSG00000276137-MIR6133 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR6133
DMDM Disease mutations102465139
Blocks (Seattle)MIR6133
Human Protein Atlas [tissue]ENSG00000276137-MIR6133 [tissue]
Protein Interaction databases
FunCoupENSG00000276137
BioGRIDMIR6133
STRING (EMBL)MIR6133
ZODIACMIR6133
Ontologies - Pathways
Huge Navigator MIR6133 [HugePedia]
snp3D : Map Gene to Disease102465139
BioCentury BCIQMIR6133
ClinGenMIR6133
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102465139
Clinical trialMIR6133
Miscellaneous
canSAR (ICR)MIR6133 (select the gene name)
DataMed IndexMIR6133
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR6133
EVEXMIR6133
GoPubMedMIR6133
iHOPMIR6133
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 : Thu Feb 14 15:46:20 CET 2019
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