Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

LINC00293 (long intergenic non-protein coding RNA 293)

Identity

Alias_namesNCRNA00293
non-protein coding RNA 293
Alias_symbol (synonym)BEYLA
Other alias
HGNC (Hugo) LINC00293
LocusID (NCBI) 497634
Atlas_Id 65347
Location 8q11.1  [Link to chromosome band 8q11]
Location_base_pair Starts at 46840886 and ends at 46855785 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)LINC00293   39078
Cards
Entrez_Gene (NCBI)LINC00293  497634  long intergenic non-protein coding RNA 293
AliasesBEYLA; NCRNA00293
GeneCards (Weizmann)LINC00293
Ensembl hg19 (Hinxton)ENSG00000253314 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000253314 [Gene_View]  chr8:46840886-46855785 [Contig_View]  LINC00293 [Vega]
ICGC DataPortalENSG00000253314
TCGA cBioPortalLINC00293
AceView (NCBI)LINC00293
Genatlas (Paris)LINC00293
WikiGenes497634
SOURCE (Princeton)LINC00293
Genetics Home Reference (NIH)LINC00293
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00293  -     chr8:46840886-46855785 +  8q11.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00293  -     8q11.1   [Description]    (hg19-Feb_2009)
EnsemblLINC00293 - 8q11.1 [CytoView hg19]  LINC00293 - 8q11.1 [CytoView hg38]
Mapping of homologs : NCBILINC00293 [Mapview hg19]  LINC00293 [Mapview hg38]
OMIM609543   
Gene and transcription
Genbank (Entrez)AK097475 BC041354
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00293
Cluster EST : UnigeneHs.406982 [ NCBI ]
CGAP (NCI)Hs.406982
Alternative Splicing GalleryENSG00000253314
Gene ExpressionLINC00293 [ NCBI-GEO ]   LINC00293 [ EBI - ARRAY_EXPRESS ]   LINC00293 [ SEEK ]   LINC00293 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00293 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)497634
GTEX Portal (Tissue expression)LINC00293
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00293
DMDM Disease mutations497634
Blocks (Seattle)LINC00293
Human Protein AtlasENSG00000253314
Protein Interaction databases
FunCoupENSG00000253314
BioGRIDLINC00293
STRING (EMBL)LINC00293
ZODIACLINC00293
Ontologies - Pathways
Huge Navigator LINC00293 [HugePedia]
snp3D : Map Gene to Disease497634
BioCentury BCIQLINC00293
ClinGenLINC00293
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD497634
Clinical trialLINC00293
Miscellaneous
canSAR (ICR)LINC00293 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00293
EVEXLINC00293
GoPubMedLINC00293
iHOPLINC00293
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 : Wed Jun 7 15:56:12 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.