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LINC02589 (long intergenic non-protein coding RNA 2589)

Identity

Other alias-
HGNC (Hugo) LINC02589
LocusID (NCBI) 105373300
Atlas_Id 80342
Location Xq22.2  [Link to chromosome band Xq22]
Location_base_pair Starts at 103530767 and ends at 103554953 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)LINC02589   53859
Cards
Entrez_Gene (NCBI)LINC02589  105373300  long intergenic non-protein coding RNA 2589
Aliases
GeneCards (Weizmann)LINC02589
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chrX:103530767-103554953 [Contig_View]  LINC02589 [Vega]
TCGA cBioPortalLINC02589
AceView (NCBI)LINC02589
Genatlas (Paris)LINC02589
WikiGenes105373300
SOURCE (Princeton)LINC02589
Genetics Home Reference (NIH)LINC02589
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02589  -     chrX:103530767-103554953 -  Xq22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02589  -     Xq22.2   [Description]    (hg19-Feb_2009)
GoldenPathLINC02589 - Xq22.2 [CytoView hg19]  LINC02589 - Xq22.2 [CytoView hg38]
Mapping of homologs : NCBILINC02589 [Mapview hg19]  LINC02589 [Mapview hg38]
Gene and transcription
Genbank (Entrez)CA392547 DA810357 DB079162
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02589
Gene ExpressionLINC02589 [ NCBI-GEO ]   LINC02589 [ EBI - ARRAY_EXPRESS ]   LINC02589 [ SEEK ]   LINC02589 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02589 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105373300
GTEX Portal (Tissue expression)LINC02589
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02589
DMDM Disease mutations105373300
Blocks (Seattle)LINC02589
Protein Interaction databases
BioGRIDLINC02589
STRING (EMBL)LINC02589
ZODIACLINC02589
Ontologies - Pathways
Huge Navigator LINC02589 [HugePedia]
snp3D : Map Gene to Disease105373300
BioCentury BCIQLINC02589
ClinGenLINC02589
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105373300
Clinical trialLINC02589
Miscellaneous
canSAR (ICR)LINC02589 (select the gene name)
DataMed IndexLINC02589
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02589
EVEXLINC02589
GoPubMedLINC02589
iHOPLINC02589
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 : Tue Sep 3 15:39:11 CEST 2019

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