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MIR5692B (microRNA 5692b)

Identity

Alias_symbol (synonym)hsa-mir-5692b
Other alias-
HGNC (Hugo) MIR5692B
LocusID (NCBI) 100847013
Atlas_Id 69886
Location 21q22.3  [Link to chromosome band 21q22]
Location_base_pair Starts at 42950928 and ends at 42951014 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)MIR5692B   43535
Cards
Entrez_Gene (NCBI)MIR5692B  100847013  microRNA 5692b
Aliases
GeneCards (Weizmann)MIR5692B
Ensembl hg19 (Hinxton)ENSG00000264580 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264580 [Gene_View]  chr21:42950928-42951014 [Contig_View]  MIR5692B [Vega]
ICGC DataPortalENSG00000264580
TCGA cBioPortalMIR5692B
AceView (NCBI)MIR5692B
Genatlas (Paris)MIR5692B
WikiGenes100847013
SOURCE (Princeton)MIR5692B
Genetics Home Reference (NIH)MIR5692B
miRBaseMIR5692B
dbDEMCMIR5692B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5692B  -     chr21:42950928-42951014 -  21q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5692B  -     21q22.3   [Description]    (hg19-Feb_2009)
EnsemblMIR5692B - 21q22.3 [CytoView hg19]  MIR5692B - 21q22.3 [CytoView hg38]
Mapping of homologs : NCBIMIR5692B [Mapview hg19]  MIR5692B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5692B
Alternative Splicing GalleryENSG00000264580
Gene ExpressionMIR5692B [ NCBI-GEO ]   MIR5692B [ EBI - ARRAY_EXPRESS ]   MIR5692B [ SEEK ]   MIR5692B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5692B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847013
GTEX Portal (Tissue expression)MIR5692B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5692B
DMDM Disease mutations100847013
Blocks (Seattle)MIR5692B
Human Protein AtlasENSG00000264580
Protein Interaction databases
FunCoupENSG00000264580
BioGRIDMIR5692B
STRING (EMBL)MIR5692B
ZODIACMIR5692B
Ontologies - Pathways
Huge Navigator MIR5692B [HugePedia]
snp3D : Map Gene to Disease100847013
BioCentury BCIQMIR5692B
ClinGenMIR5692B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847013
Clinical trialMIR5692B
Miscellaneous
canSAR (ICR)MIR5692B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5692B
EVEXMIR5692B
GoPubMedMIR5692B
iHOPMIR5692B
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 15:29:33 CEST 2017

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