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LINC02490 (long intergenic non-protein coding RNA 2490)

Identity

Alias_symbol (synonym)RP11-209E8
Other alias-
HGNC (Hugo) LINC02490
LocusID (NCBI) 105370822
Atlas_Id 79094
Location 15q21.3  [Link to chromosome band 15q21]
Location_base_pair Starts at 53116365 and ends at 53129698 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


External links

Nomenclature
HGNC (Hugo)LINC02490   53471
Cards
Entrez_Gene (NCBI)LINC02490  105370822  long intergenic non-protein coding RNA 2490
Aliases
GeneCards (Weizmann)LINC02490
Ensembl hg19 (Hinxton)ENSG00000259237 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000259237 [Gene_View]  chr15:53116365-53129698 [Contig_View]  LINC02490 [Vega]
ICGC DataPortalENSG00000259237
TCGA cBioPortalLINC02490
AceView (NCBI)LINC02490
Genatlas (Paris)LINC02490
WikiGenes105370822
SOURCE (Princeton)LINC02490
Genetics Home Reference (NIH)LINC02490
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02490  -     chr15:53116365-53129698 +  15q21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02490  -     15q21.3   [Description]    (hg19-Feb_2009)
EnsemblLINC02490 - 15q21.3 [CytoView hg19]  LINC02490 - 15q21.3 [CytoView hg38]
Mapping of homologs : NCBILINC02490 [Mapview hg19]  LINC02490 [Mapview hg38]
Gene and transcription
Genbank (Entrez)CF595856
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02490
Cluster EST : UnigeneHs.527821 [ NCBI ]
CGAP (NCI)Hs.527821
Alternative Splicing GalleryENSG00000259237
Gene ExpressionLINC02490 [ NCBI-GEO ]   LINC02490 [ EBI - ARRAY_EXPRESS ]   LINC02490 [ SEEK ]   LINC02490 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02490 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105370822
GTEX Portal (Tissue expression)LINC02490
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02490
DMDM Disease mutations105370822
Blocks (Seattle)LINC02490
Human Protein AtlasENSG00000259237
Protein Interaction databases
FunCoupENSG00000259237
BioGRIDLINC02490
STRING (EMBL)LINC02490
ZODIACLINC02490
Ontologies - Pathways
Huge Navigator LINC02490 [HugePedia]
snp3D : Map Gene to Disease105370822
BioCentury BCIQLINC02490
ClinGenLINC02490
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105370822
Clinical trialLINC02490
Miscellaneous
canSAR (ICR)LINC02490 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02490
EVEXLINC02490
GoPubMedLINC02490
iHOPLINC02490
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Sep 18 13:16:33 CEST 2017

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