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MIR487B (microRNA 487b)

Identity

Alias_namesMIRN487B
Alias_symbol (synonym)hsa-mir-487b
Other aliasmir-487b
HGNC (Hugo) MIR487B
LocusID (NCBI) 664616
Atlas_Id 53344
Location 14q32.31  [Link to chromosome band 14q32]
Location_base_pair Starts at 101046455 and ends at 101046538 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)MIR487B   32533
Cards
Entrez_Gene (NCBI)MIR487B  664616  microRNA 487b
AliasesMIRN487B; mir-487b
GeneCards (Weizmann)MIR487B
Ensembl hg19 (Hinxton)ENSG00000207754 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207754 [Gene_View]  ENSG00000207754 [Sequence]  chr14:101046455-101046538 [Contig_View]  MIR487B [Vega]
ICGC DataPortalENSG00000207754
TCGA cBioPortalMIR487B
AceView (NCBI)MIR487B
Genatlas (Paris)MIR487B
WikiGenes664616
SOURCE (Princeton)MIR487B
Genetics Home Reference (NIH)MIR487B
miRBaseMIR487B
dbDEMCMIR487B
Genomic and cartography
GoldenPath hg38 (UCSC)MIR487B  -     chr14:101046455-101046538 +  14q32.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR487B  -     14q32.31   [Description]    (hg19-Feb_2009)
MIR487B - 14q32.31 [CytoView hg19]  MIR487B - 14q32.31 [CytoView hg38]
Mapping of homologs : NCBIMIR487B [Mapview hg19]  MIR487B [Mapview hg38]
OMIM615037   
Gene and transcription
Genbank (Entrez)LM609537
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR487B
Alternative Splicing GalleryENSG00000207754
Gene ExpressionMIR487B [ NCBI-GEO ]   MIR487B [ EBI - ARRAY_EXPRESS ]   MIR487B [ SEEK ]   MIR487B [ MEM ]
Gene Expression Viewer (FireBrowse)MIR487B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)664616
GTEX Portal (Tissue expression)MIR487B
Human Protein AtlasENSG00000207754-MIR487B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR487B
DMDM Disease mutations664616
Blocks (Seattle)MIR487B
Human Protein Atlas [tissue]ENSG00000207754-MIR487B [tissue]
Protein Interaction databases
FunCoupENSG00000207754
BioGRIDMIR487B
STRING (EMBL)MIR487B
ZODIACMIR487B
Ontologies - Pathways
Huge Navigator MIR487B [HugePedia]
snp3D : Map Gene to Disease664616
BioCentury BCIQMIR487B
ClinGenMIR487B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD664616
Chemical/Pharm GKB GenePA164722733
Clinical trialMIR487B
Miscellaneous
canSAR (ICR)MIR487B (select the gene name)
DataMed IndexMIR487B
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR487B
EVEXMIR487B
GoPubMedMIR487B
iHOPMIR487B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu May 2 12:59:10 CEST 2019

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