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DINOL (damage induced long noncoding RNA)

Identity

Alias (NCBI)DINO
HGNC (Hugo) DINOL
HGNC Alias symbDINO
HGNC Alias namedamage induced noncoding
LocusID (NCBI) 108783646
Atlas_Id 80080
Location 6p21.2  [Link to chromosome band 6p21]
Location_base_pair Starts at 36677609 and ends at 36678559 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


External links

Nomenclature
HGNC (Hugo)DINOL   53146
Cards
Entrez_Gene (NCBI)DINOL  108783646  damage induced long noncoding RNA
AliasesDINO
GeneCards (Weizmann)DINOL
Ensembl hg19 (Hinxton)ENSG00000285244 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000285244 [Gene_View]  ENSG00000285244 [Sequence]  chr6:36677609-36678559 [Contig_View]  DINOL [Vega]
ICGC DataPortalENSG00000285244
TCGA cBioPortalDINOL
AceView (NCBI)DINOL
Genatlas (Paris)DINOL
WikiGenes108783646
SOURCE (Princeton)DINOL
Genetics Home Reference (NIH)DINOL
Genomic and cartography
GoldenPath hg38 (UCSC)DINOL  -     chr6:36677609-36678559 -  6p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DINOL  -     6p21.2   [Description]    (hg19-Feb_2009)
GoldenPathDINOL - 6p21.2 [CytoView hg19]  DINOL - 6p21.2 [CytoView hg38]
ImmunoBaseENSG00000285244
genome Data Viewer NCBIDINOL [Mapview hg19]  
Gene and transcription
Genbank (Entrez)JX993265
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)DINOL
Alternative Splicing GalleryENSG00000285244
Gene ExpressionDINOL [ NCBI-GEO ]   DINOL [ EBI - ARRAY_EXPRESS ]   DINOL [ SEEK ]   DINOL [ MEM ]
Gene Expression Viewer (FireBrowse)DINOL [ Firebrowse - Broad ]
GenevisibleExpression of DINOL in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)108783646
GTEX Portal (Tissue expression)DINOL
Human Protein AtlasENSG00000285244-DINOL [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)DINOL
DMDM Disease mutations108783646
Blocks (Seattle)DINOL
Human Protein Atlas [tissue]ENSG00000285244-DINOL [tissue]
Protein Interaction databases
FunCoupENSG00000285244
BioGRIDDINOL
STRING (EMBL)DINOL
ZODIACDINOL
Ontologies - Pathways
Huge Navigator DINOL [HugePedia]
snp3D : Map Gene to Disease108783646
BioCentury BCIQDINOL
ClinGenDINOL
Clinical trials, drugs, therapy
Protein Interactions : CTD108783646
Clinical trialDINOL
Miscellaneous
canSAR (ICR)DINOL (select the gene name)
HarmonizomeDINOL
DataMed IndexDINOL
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDINOL
EVEXDINOL
GoPubMedDINOL
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Aug 22 19:09:59 CEST 2020

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