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LINC01867 (long intergenic non-protein coding RNA 1867)

Identity

Other alias-
HGNC (Hugo) LINC01867
LocusID (NCBI) 105374596
Atlas_Id 79071
Location 2p16.3  [Link to chromosome band 2p16]
Location_base_pair Starts at 52370648 and ends at 52390070 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)LINC01867   52687
Cards
Entrez_Gene (NCBI)LINC01867  105374596  long intergenic non-protein coding RNA 1867
Aliases
GeneCards (Weizmann)LINC01867
Ensembl hg19 (Hinxton)ENSG00000225444 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000225444 [Gene_View]  chr2:52370648-52390070 [Contig_View]  LINC01867 [Vega]
ICGC DataPortalENSG00000225444
TCGA cBioPortalLINC01867
AceView (NCBI)LINC01867
Genatlas (Paris)LINC01867
WikiGenes105374596
SOURCE (Princeton)LINC01867
Genetics Home Reference (NIH)LINC01867
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01867  -     chr2:52370648-52390070 +  2p16.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01867  -     2p16.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01867 - 2p16.3 [CytoView hg19]  LINC01867 - 2p16.3 [CytoView hg38]
Mapping of homologs : NCBILINC01867 [Mapview hg19]  LINC01867 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01867
Alternative Splicing GalleryENSG00000225444
Gene ExpressionLINC01867 [ NCBI-GEO ]   LINC01867 [ EBI - ARRAY_EXPRESS ]   LINC01867 [ SEEK ]   LINC01867 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01867 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105374596
GTEX Portal (Tissue expression)LINC01867
Human Protein AtlasENSG00000225444-LINC01867 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01867
DMDM Disease mutations105374596
Blocks (Seattle)LINC01867
Human Protein Atlas [tissue]ENSG00000225444-LINC01867 [tissue]
Protein Interaction databases
FunCoupENSG00000225444
BioGRIDLINC01867
STRING (EMBL)LINC01867
ZODIACLINC01867
Ontologies - Pathways
Huge Navigator LINC01867 [HugePedia]
snp3D : Map Gene to Disease105374596
BioCentury BCIQLINC01867
ClinGenLINC01867
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105374596
Clinical trialLINC01867
Miscellaneous
canSAR (ICR)LINC01867 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01867
EVEXLINC01867
GoPubMedLINC01867
iHOPLINC01867
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 Nov 21 13:05:13 CET 2017

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