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LINC02587 (long intergenic non-protein coding RNA 2587)

Identity

Other aliasMEOX2-AS1
HGNC (Hugo) LINC02587
LocusID (NCBI) 101927524
Atlas_Id 80407
Location 7p21.2  [Link to chromosome band 7p21]
Location_base_pair Starts at 15688378 and ends at 15696892 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


External links

Nomenclature
HGNC (Hugo)LINC02587   50672
Cards
Entrez_Gene (NCBI)LINC02587  101927524  long intergenic non-protein coding RNA 2587
AliasesMEOX2-AS1
GeneCards (Weizmann)LINC02587
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr7:15688378-15696892 [Contig_View]  LINC02587 [Vega]
TCGA cBioPortalLINC02587
AceView (NCBI)LINC02587
Genatlas (Paris)LINC02587
WikiGenes101927524
SOURCE (Princeton)LINC02587
Genetics Home Reference (NIH)LINC02587
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02587  -     chr7:15688378-15696892 +  7p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02587  -     7p21.2   [Description]    (hg19-Feb_2009)
GoldenPathLINC02587 - 7p21.2 [CytoView hg19]  LINC02587 - 7p21.2 [CytoView hg38]
genome Data Viewer NCBILINC02587 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AI263603 DA829065
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02587
Gene ExpressionLINC02587 [ NCBI-GEO ]   LINC02587 [ EBI - ARRAY_EXPRESS ]   LINC02587 [ SEEK ]   LINC02587 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02587 [ Firebrowse - Broad ]
GenevisibleExpression of LINC02587 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101927524
GTEX Portal (Tissue expression)LINC02587
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02587
DMDM Disease mutations101927524
Blocks (Seattle)LINC02587
Protein Interaction databases
BioGRIDLINC02587
STRING (EMBL)LINC02587
ZODIACLINC02587
Ontologies - Pathways
Huge Navigator LINC02587 [HugePedia]
snp3D : Map Gene to Disease101927524
BioCentury BCIQLINC02587
ClinGenLINC02587
Clinical trials, drugs, therapy
Protein Interactions : CTD101927524
Clinical trialLINC02587
Miscellaneous
canSAR (ICR)LINC02587 (select the gene name)
HarmonizomeLINC02587
DataMed IndexLINC02587
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02587
EVEXLINC02587
GoPubMedLINC02587
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 : Fri Jul 10 20:14:24 CEST 2020

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