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LINC02091 (long intergenic non-protein coding RNA 2091)

Identity

Other alias-
HGNC (Hugo) LINC02091
LocusID (NCBI) 100506371
Atlas_Id 79649
Location 17p13.3  [Link to chromosome band 17p13]
Location_base_pair Starts at 183824 and ends at 187251 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)LINC02091   52942
Cards
Entrez_Gene (NCBI)LINC02091  100506371  long intergenic non-protein coding RNA 2091
Aliases
GeneCards (Weizmann)LINC02091
Ensembl hg19 (Hinxton)ENSG00000273172 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000273172 [Gene_View]  chr17:183824-187251 [Contig_View]  LINC02091 [Vega]
ICGC DataPortalENSG00000273172
TCGA cBioPortalLINC02091
AceView (NCBI)LINC02091
Genatlas (Paris)LINC02091
WikiGenes100506371
SOURCE (Princeton)LINC02091
Genetics Home Reference (NIH)LINC02091
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02091  -     chr17:183824-187251 -  17p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02091  -     17p13.3   [Description]    (hg19-Feb_2009)
EnsemblLINC02091 - 17p13.3 [CytoView hg19]  LINC02091 - 17p13.3 [CytoView hg38]
Mapping of homologs : NCBILINC02091 [Mapview hg19]  LINC02091 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02091
Alternative Splicing GalleryENSG00000273172
Gene ExpressionLINC02091 [ NCBI-GEO ]   LINC02091 [ EBI - ARRAY_EXPRESS ]   LINC02091 [ SEEK ]   LINC02091 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02091 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506371
GTEX Portal (Tissue expression)LINC02091
Human Protein AtlasENSG00000273172-LINC02091 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02091
DMDM Disease mutations100506371
Blocks (Seattle)LINC02091
Human Protein Atlas [tissue]ENSG00000273172-LINC02091 [tissue]
Protein Interaction databases
FunCoupENSG00000273172
BioGRIDLINC02091
STRING (EMBL)LINC02091
ZODIACLINC02091
Ontologies - Pathways
Huge Navigator LINC02091 [HugePedia]
snp3D : Map Gene to Disease100506371
BioCentury BCIQLINC02091
ClinGenLINC02091
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506371
Clinical trialLINC02091
Miscellaneous
canSAR (ICR)LINC02091 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02091
EVEXLINC02091
GoPubMedLINC02091
iHOPLINC02091
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 Nov 21 13:35:54 CET 2017

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