Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR1587 (microRNA 1587)

Identity

Alias_symbol (synonym)hsa-mir-1587
Other alias-
HGNC (Hugo) MIR1587
LocusID (NCBI) 100616251
Atlas_Id 79548
Location Xp11.4  [Link to chromosome band Xp11]
Location_base_pair Starts at 39837561 and ends at 39837613 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)MIR1587   41596
Cards
Entrez_Gene (NCBI)MIR1587  100616251  microRNA 1587
Aliases
GeneCards (Weizmann)MIR1587
Ensembl hg19 (Hinxton)ENSG00000263972 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263972 [Gene_View]  chrX:39837561-39837613 [Contig_View]  MIR1587 [Vega]
ICGC DataPortalENSG00000263972
TCGA cBioPortalMIR1587
AceView (NCBI)MIR1587
Genatlas (Paris)MIR1587
WikiGenes100616251
SOURCE (Princeton)MIR1587
Genetics Home Reference (NIH)MIR1587
miRBaseMIR1587
dbDEMCMIR1587
Genomic and cartography
GoldenPath hg38 (UCSC)MIR1587  -     chrX:39837561-39837613 +  Xp11.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR1587  -     Xp11.4   [Description]    (hg19-Feb_2009)
EnsemblMIR1587 - Xp11.4 [CytoView hg19]  MIR1587 - Xp11.4 [CytoView hg38]
Mapping of homologs : NCBIMIR1587 [Mapview hg19]  MIR1587 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR1587
Alternative Splicing GalleryENSG00000263972
Gene ExpressionMIR1587 [ NCBI-GEO ]   MIR1587 [ EBI - ARRAY_EXPRESS ]   MIR1587 [ SEEK ]   MIR1587 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR1587 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616251
GTEX Portal (Tissue expression)MIR1587
Human Protein AtlasENSG00000263972-MIR1587 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR1587
DMDM Disease mutations100616251
Blocks (Seattle)MIR1587
Human Protein Atlas [tissue]ENSG00000263972-MIR1587 [tissue]
Protein Interaction databases
FunCoupENSG00000263972
BioGRIDMIR1587
STRING (EMBL)MIR1587
ZODIACMIR1587
Ontologies - Pathways
Huge Navigator MIR1587 [HugePedia]
snp3D : Map Gene to Disease100616251
BioCentury BCIQMIR1587
ClinGenMIR1587
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616251
Clinical trialMIR1587
Miscellaneous
canSAR (ICR)MIR1587 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR1587
EVEXMIR1587
GoPubMedMIR1587
iHOPMIR1587
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 : Mon Nov 20 19:57:00 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.