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LINC02022 (long intergenic non-protein coding RNA 2022)

Identity

Other alias-
HGNC (Hugo) LINC02022
LocusID (NCBI) 105376955
Atlas_Id 79913
Location 3p25.2  [Link to chromosome band 3p25]
Location_base_pair Starts at 12877522 and ends at 12885211 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)LINC02022   52857
Cards
Entrez_Gene (NCBI)LINC02022  105376955  long intergenic non-protein coding RNA 2022
Aliases
GeneCards (Weizmann)LINC02022
Ensembl hg19 (Hinxton)ENSG00000232746 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232746 [Gene_View]  ENSG00000232746 [Sequence]  chr3:12877522-12885211 [Contig_View]  LINC02022 [Vega]
ICGC DataPortalENSG00000232746
TCGA cBioPortalLINC02022
AceView (NCBI)LINC02022
Genatlas (Paris)LINC02022
WikiGenes105376955
SOURCE (Princeton)LINC02022
Genetics Home Reference (NIH)LINC02022
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02022  -     chr3:12877522-12885211 -  3p25.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02022  -     3p25.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02022 - 3p25.2 [CytoView hg19]  LINC02022 - 3p25.2 [CytoView hg38]
Mapping of homologs : NCBILINC02022 [Mapview hg19]  LINC02022 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG759368
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02022
Cluster EST : UnigeneHs.561179 [ NCBI ]
CGAP (NCI)Hs.561179
Alternative Splicing GalleryENSG00000232746
Gene ExpressionLINC02022 [ NCBI-GEO ]   LINC02022 [ EBI - ARRAY_EXPRESS ]   LINC02022 [ SEEK ]   LINC02022 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02022 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105376955
GTEX Portal (Tissue expression)LINC02022
Human Protein AtlasENSG00000232746-LINC02022 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02022
DMDM Disease mutations105376955
Blocks (Seattle)LINC02022
Human Protein Atlas [tissue]ENSG00000232746-LINC02022 [tissue]
Protein Interaction databases
FunCoupENSG00000232746
BioGRIDLINC02022
STRING (EMBL)LINC02022
ZODIACLINC02022
Ontologies - Pathways
Huge Navigator LINC02022 [HugePedia]
snp3D : Map Gene to Disease105376955
BioCentury BCIQLINC02022
ClinGenLINC02022
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105376955
Clinical trialLINC02022
Miscellaneous
canSAR (ICR)LINC02022 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02022
EVEXLINC02022
GoPubMedLINC02022
iHOPLINC02022
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 13:56:42 CEST 2018

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