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NORAD (non-coding RNA activated by DNA damage)

Identity

Alias_namesLINC00657
long intergenic non-protein coding RNA 657
Other alias
HGNC (Hugo) NORAD
LocusID (NCBI) 647979
Atlas_Id 77939
Location 20q11.23  [Link to chromosome band 20q11]
Location_base_pair Starts at 36045618 and ends at 36050960 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)NORAD   44311
Cards
Entrez_Gene (NCBI)NORAD  647979  non-coding RNA activated by DNA damage
AliasesLINC00657
GeneCards (Weizmann)NORAD
Ensembl hg19 (Hinxton)ENSG00000260032 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000260032 [Gene_View]  chr20:36045618-36050960 [Contig_View]  NORAD [Vega]
ICGC DataPortalENSG00000260032
TCGA cBioPortalNORAD
AceView (NCBI)NORAD
Genatlas (Paris)NORAD
WikiGenes647979
SOURCE (Princeton)NORAD
Genetics Home Reference (NIH)NORAD
Genomic and cartography
GoldenPath hg38 (UCSC)NORAD  -     chr20:36045618-36050960 -  20q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NORAD  -     20q11.23   [Description]    (hg19-Feb_2009)
EnsemblNORAD - 20q11.23 [CytoView hg19]  NORAD - 20q11.23 [CytoView hg38]
Mapping of homologs : NCBINORAD [Mapview hg19]  NORAD [Mapview hg38]
OMIM617037   
Gene and transcription
Genbank (Entrez)AI619767 AK090641 BC011592
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)NORAD
Cluster EST : UnigeneHs.743232 [ NCBI ]
CGAP (NCI)Hs.743232
Alternative Splicing GalleryENSG00000260032
Gene ExpressionNORAD [ NCBI-GEO ]   NORAD [ EBI - ARRAY_EXPRESS ]   NORAD [ SEEK ]   NORAD [ MEM ]
Gene Expression Viewer (FireBrowse)NORAD [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)647979
GTEX Portal (Tissue expression)NORAD
Human Protein AtlasENSG00000260032-NORAD [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)NORAD
DMDM Disease mutations647979
Blocks (Seattle)NORAD
Human Protein Atlas [tissue]ENSG00000260032-NORAD [tissue]
IPIIPI00981422   
Protein Interaction databases
FunCoupENSG00000260032
BioGRIDNORAD
STRING (EMBL)NORAD
ZODIACNORAD
Ontologies - Pathways
Huge Navigator NORAD [HugePedia]
snp3D : Map Gene to Disease647979
BioCentury BCIQNORAD
ClinGenNORAD
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD647979
Clinical trialNORAD
Miscellaneous
canSAR (ICR)NORAD (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNORAD
EVEXNORAD
GoPubMedNORAD
iHOPNORAD
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 : Thu Nov 9 12:19:12 CET 2017

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