Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR892B (microRNA 892b)

Identity

Alias_namesMIRN892B
Alias_symbol (synonym)hsa-mir-892b
Other alias
HGNC (Hugo) MIR892B
LocusID (NCBI) 100126307
Atlas_Id 55869
Location Xq27.3  [Link to chromosome band Xq27]
Location_base_pair Starts at 145997198 and ends at 145997274 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)MIR892B   33649
Cards
Entrez_Gene (NCBI)MIR892B  100126307  microRNA 892b
AliasesMIRN892B
GeneCards (Weizmann)MIR892B
Ensembl hg19 (Hinxton)ENSG00000216098 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000216098 [Gene_View]  chrX:145997198-145997274 [Contig_View]  MIR892B [Vega]
ICGC DataPortalENSG00000216098
TCGA cBioPortalMIR892B
AceView (NCBI)MIR892B
Genatlas (Paris)MIR892B
WikiGenes100126307
SOURCE (Princeton)MIR892B
Genetics Home Reference (NIH)MIR892B
miRBaseMIR892B
dbDEMCMIR892B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR892B  -     chrX:145997198-145997274 -  Xq27.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR892B  -     Xq27.3   [Description]    (hg19-Feb_2009)
EnsemblMIR892B - Xq27.3 [CytoView hg19]  MIR892B - Xq27.3 [CytoView hg38]
Mapping of homologs : NCBIMIR892B [Mapview hg19]  MIR892B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR892B
Alternative Splicing GalleryENSG00000216098
Gene ExpressionMIR892B [ NCBI-GEO ]   MIR892B [ EBI - ARRAY_EXPRESS ]   MIR892B [ SEEK ]   MIR892B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR892B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100126307
GTEX Portal (Tissue expression)MIR892B
Human Protein AtlasENSG00000216098-MIR892B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR892B
DMDM Disease mutations100126307
Blocks (Seattle)MIR892B
Human Protein Atlas [tissue]ENSG00000216098-MIR892B [tissue]
Protein Interaction databases
FunCoupENSG00000216098
BioGRIDMIR892B
STRING (EMBL)MIR892B
ZODIACMIR892B
Ontologies - Pathways
Huge Navigator MIR892B [HugePedia]
snp3D : Map Gene to Disease100126307
BioCentury BCIQMIR892B
ClinGenMIR892B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100126307
Chemical/Pharm GKB GenePA164722994
Clinical trialMIR892B
Miscellaneous
canSAR (ICR)MIR892B (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR892B
EVEXMIR892B
GoPubMedMIR892B
iHOPMIR892B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 14:24:18 CET 2017

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