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LINC00867 (long intergenic non-protein coding RNA 867)

Identity

Other alias-
HGNC (Hugo) LINC00867
LocusID (NCBI) 100506126
Atlas_Id 65633
Location 10q26.11  [Link to chromosome band 10q26]
Location_base_pair Starts at 118357108 and ends at 118359203 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)LINC00867   45265
Cards
Entrez_Gene (NCBI)LINC00867  100506126  long intergenic non-protein coding RNA 867
Aliases
GeneCards (Weizmann)LINC00867
Ensembl hg19 (Hinxton)ENSG00000232139 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232139 [Gene_View]  chr10:118357108-118359203 [Contig_View]  LINC00867 [Vega]
ICGC DataPortalENSG00000232139
TCGA cBioPortalLINC00867
AceView (NCBI)LINC00867
Genatlas (Paris)LINC00867
WikiGenes100506126
SOURCE (Princeton)LINC00867
Genetics Home Reference (NIH)LINC00867
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00867  -     chr10:118357108-118359203 +  10q26.11   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00867  -     10q26.11   [Description]    (hg19-Feb_2009)
EnsemblLINC00867 - 10q26.11 [CytoView hg19]  LINC00867 - 10q26.11 [CytoView hg38]
Mapping of homologs : NCBILINC00867 [Mapview hg19]  LINC00867 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA121564 AI187845 AI733769
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00867
Cluster EST : UnigeneHs.69494 [ NCBI ]
CGAP (NCI)Hs.69494
Alternative Splicing GalleryENSG00000232139
Gene ExpressionLINC00867 [ NCBI-GEO ]   LINC00867 [ EBI - ARRAY_EXPRESS ]   LINC00867 [ SEEK ]   LINC00867 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00867 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506126
GTEX Portal (Tissue expression)LINC00867
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00867
DMDM Disease mutations100506126
Blocks (Seattle)LINC00867
Human Protein AtlasENSG00000232139
Protein Interaction databases
FunCoupENSG00000232139
BioGRIDLINC00867
STRING (EMBL)LINC00867
ZODIACLINC00867
Ontologies - Pathways
Huge Navigator LINC00867 [HugePedia]
snp3D : Map Gene to Disease100506126
BioCentury BCIQLINC00867
ClinGenLINC00867
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506126
Clinical trialLINC00867
Miscellaneous
canSAR (ICR)LINC00867 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00867
EVEXLINC00867
GoPubMedLINC00867
iHOPLINC00867
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 : Wed Jun 7 15:57:27 CEST 2017

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