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LINC02568 (long intergenic non-protein coding RNA 2568)

Identity

Other alias-
HGNC (Hugo) LINC02568
LocusID (NCBI) 102723344
Atlas_Id 79512
Location 15q22.2  [Link to chromosome band 15q22]
Location_base_pair Starts at 63390230 and ends at 63437536 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)LINC02568   51430
Cards
Entrez_Gene (NCBI)LINC02568  102723344  long intergenic non-protein coding RNA 2568
Aliases
GeneCards (Weizmann)LINC02568
Ensembl hg19 (Hinxton)ENSG00000259459 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000259459 [Gene_View]  chr15:63390230-63437536 [Contig_View]  LINC02568 [Vega]
ICGC DataPortalENSG00000259459
TCGA cBioPortalLINC02568
AceView (NCBI)LINC02568
Genatlas (Paris)LINC02568
WikiGenes102723344
SOURCE (Princeton)LINC02568
Genetics Home Reference (NIH)LINC02568
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02568  -     chr15:63390230-63437536 +  15q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02568  -     15q22.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02568 - 15q22.2 [CytoView hg19]  LINC02568 - 15q22.2 [CytoView hg38]
Mapping of homologs : NCBILINC02568 [Mapview hg19]  LINC02568 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG675369 BX642193
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02568
Cluster EST : UnigeneHs.569500 [ NCBI ]
CGAP (NCI)Hs.569500
Alternative Splicing GalleryENSG00000259459
Gene ExpressionLINC02568 [ NCBI-GEO ]   LINC02568 [ EBI - ARRAY_EXPRESS ]   LINC02568 [ SEEK ]   LINC02568 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02568 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102723344
GTEX Portal (Tissue expression)LINC02568
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02568
DMDM Disease mutations102723344
Blocks (Seattle)LINC02568
Human Protein AtlasENSG00000259459
Protein Interaction databases
FunCoupENSG00000259459
BioGRIDLINC02568
STRING (EMBL)LINC02568
ZODIACLINC02568
Ontologies - Pathways
Huge Navigator LINC02568 [HugePedia]
snp3D : Map Gene to Disease102723344
BioCentury BCIQLINC02568
ClinGenLINC02568
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102723344
Clinical trialLINC02568
Miscellaneous
canSAR (ICR)LINC02568 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02568
EVEXLINC02568
GoPubMedLINC02568
iHOPLINC02568
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 Sep 18 13:16:39 CEST 2017

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