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LINC00863 (long intergenic non-protein coding RNA 863)

Identity

Other alias-
HGNC (Hugo) LINC00863
LocusID (NCBI) 439994
Atlas_Id 65629
Location 10q23.2  [Link to chromosome band 10q23]
Location_base_pair Starts at 87342411 and ends at 87343574 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)LINC00863   45162
Cards
Entrez_Gene (NCBI)LINC00863  439994  long intergenic non-protein coding RNA 863
Aliases
GeneCards (Weizmann)LINC00863
Ensembl hg19 (Hinxton)ENSG00000224914 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000224914 [Gene_View]  ENSG00000224914 [Sequence]  chr10:87342411-87343574 [Contig_View]  LINC00863 [Vega]
ICGC DataPortalENSG00000224914
TCGA cBioPortalLINC00863
AceView (NCBI)LINC00863
Genatlas (Paris)LINC00863
WikiGenes439994
SOURCE (Princeton)LINC00863
Genetics Home Reference (NIH)LINC00863
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00863  -     chr10:87342411-87343574 +  10q23.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00863  -     10q23.2   [Description]    (hg19-Feb_2009)
GoldenPathLINC00863 - 10q23.2 [CytoView hg19]  LINC00863 - 10q23.2 [CytoView hg38]
ImmunoBaseENSG00000224914
Mapping of homologs : NCBILINC00863 [Mapview hg19]  LINC00863 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC082979 BG473198 CA439404 CA444075 CD369599
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00863
Cluster EST : UnigeneHs.729096 [ NCBI ]
CGAP (NCI)Hs.729096
Alternative Splicing GalleryENSG00000224914
Gene ExpressionLINC00863 [ NCBI-GEO ]   LINC00863 [ EBI - ARRAY_EXPRESS ]   LINC00863 [ SEEK ]   LINC00863 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00863 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)439994
GTEX Portal (Tissue expression)LINC00863
Human Protein AtlasENSG00000224914-LINC00863 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00863
DMDM Disease mutations439994
Blocks (Seattle)LINC00863
Human Protein Atlas [tissue]ENSG00000224914-LINC00863 [tissue]
Protein Interaction databases
FunCoupENSG00000224914
BioGRIDLINC00863
STRING (EMBL)LINC00863
ZODIACLINC00863
Ontologies - Pathways
Huge Navigator LINC00863 [HugePedia]
snp3D : Map Gene to Disease439994
BioCentury BCIQLINC00863
ClinGenLINC00863
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD439994
Clinical trialLINC00863
Miscellaneous
canSAR (ICR)LINC00863 (select the gene name)
DataMed IndexLINC00863
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00863
EVEXLINC00863
GoPubMedLINC00863
iHOPLINC00863
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Sep 3 15:35:05 CEST 2019

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