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LINC00866 (long intergenic non-protein coding RNA 866)

Identity

Other alias-
HGNC (Hugo) LINC00866
LocusID (NCBI) 100505561
Atlas_Id 65632
Location 10q24.2  [Link to chromosome band 10q24]
Location_base_pair Starts at 97828478 and ends at 97849798 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)LINC00866   45232
Cards
Entrez_Gene (NCBI)LINC00866  100505561  long intergenic non-protein coding RNA 866
Aliases
GeneCards (Weizmann)LINC00866
Ensembl hg19 (Hinxton)ENSG00000227356 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000227356 [Gene_View]  chr10:97828478-97849798 [Contig_View]  LINC00866 [Vega]
ICGC DataPortalENSG00000227356
TCGA cBioPortalLINC00866
AceView (NCBI)LINC00866
Genatlas (Paris)LINC00866
WikiGenes100505561
SOURCE (Princeton)LINC00866
Genetics Home Reference (NIH)LINC00866
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00866  -     chr10:97828478-97849798 -  10q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00866  -     10q24.2   [Description]    (hg19-Feb_2009)
EnsemblLINC00866 - 10q24.2 [CytoView hg19]  LINC00866 - 10q24.2 [CytoView hg38]
Mapping of homologs : NCBILINC00866 [Mapview hg19]  LINC00866 [Mapview hg38]
Gene and transcription
Genbank (Entrez)CK818728
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00866
Cluster EST : UnigeneHs.351904 [ NCBI ]
CGAP (NCI)Hs.351904
Alternative Splicing GalleryENSG00000227356
Gene ExpressionLINC00866 [ NCBI-GEO ]   LINC00866 [ EBI - ARRAY_EXPRESS ]   LINC00866 [ SEEK ]   LINC00866 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00866 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505561
GTEX Portal (Tissue expression)LINC00866
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00866
DMDM Disease mutations100505561
Blocks (Seattle)LINC00866
Human Protein AtlasENSG00000227356
Protein Interaction databases
FunCoupENSG00000227356
BioGRIDLINC00866
STRING (EMBL)LINC00866
ZODIACLINC00866
Ontologies - Pathways
Huge Navigator LINC00866 [HugePedia]
snp3D : Map Gene to Disease100505561
BioCentury BCIQLINC00866
ClinGenLINC00866
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505561
Clinical trialLINC00866
Miscellaneous
canSAR (ICR)LINC00866 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00866
EVEXLINC00866
GoPubMedLINC00866
iHOPLINC00866
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 13:13:39 CEST 2017

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