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LINC02567 (long intergenic non-protein coding RNA 2567)

Identity

Other alias-
HGNC (Hugo) LINC02567
LocusID (NCBI) 110806286
Atlas_Id 80433
Location 1p31.1  [Link to chromosome band 1p31]
Location_base_pair Starts at 76758124 and ends at 76779267 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)LINC02567   53609
Cards
Entrez_Gene (NCBI)LINC02567  110806286  long intergenic non-protein coding RNA 2567
Aliases
GeneCards (Weizmann)LINC02567
Ensembl hg19 (Hinxton)ENSG00000237552 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000237552 [Gene_View]  ENSG00000237552 [Sequence]  chr1:76758124-76779267 [Contig_View]  LINC02567 [Vega]
ICGC DataPortalENSG00000237552
TCGA cBioPortalLINC02567
AceView (NCBI)LINC02567
Genatlas (Paris)LINC02567
WikiGenes110806286
SOURCE (Princeton)LINC02567
Genetics Home Reference (NIH)LINC02567
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02567  -     chr1:76758124-76779267 -  1p31.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02567  -     1p31.1   [Description]    (hg19-Feb_2009)
GoldenPathLINC02567 - 1p31.1 [CytoView hg19]  LINC02567 - 1p31.1 [CytoView hg38]
ImmunoBaseENSG00000237552
Mapping of homologs : NCBILINC02567 [Mapview hg19]  LINC02567 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA062599
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02567
Alternative Splicing GalleryENSG00000237552
Gene ExpressionLINC02567 [ NCBI-GEO ]   LINC02567 [ EBI - ARRAY_EXPRESS ]   LINC02567 [ SEEK ]   LINC02567 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02567 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)110806286
GTEX Portal (Tissue expression)LINC02567
Human Protein AtlasENSG00000237552-LINC02567 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02567
DMDM Disease mutations110806286
Blocks (Seattle)LINC02567
Human Protein Atlas [tissue]ENSG00000237552-LINC02567 [tissue]
Protein Interaction databases
FunCoupENSG00000237552
BioGRIDLINC02567
STRING (EMBL)LINC02567
ZODIACLINC02567
Ontologies - Pathways
Huge Navigator LINC02567 [HugePedia]
snp3D : Map Gene to Disease110806286
BioCentury BCIQLINC02567
ClinGenLINC02567
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD110806286
Clinical trialLINC02567
Miscellaneous
canSAR (ICR)LINC02567 (select the gene name)
DataMed IndexLINC02567
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02567
EVEXLINC02567
GoPubMedLINC02567
iHOPLINC02567
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 : Tue Sep 3 15:39:07 CEST 2019

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