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LINC02190 (long intergenic non-protein coding RNA 2190)

Identity

Other alias-
HGNC (Hugo) LINC02190
LocusID (NCBI) 105371173
Atlas_Id 79778
Location 16p11.2  [Link to chromosome band 16p11]
Location_base_pair Starts at 31546698 and ends at 31553567 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)LINC02190   53052
Cards
Entrez_Gene (NCBI)LINC02190  105371173  long intergenic non-protein coding RNA 2190
Aliases
GeneCards (Weizmann)LINC02190
Ensembl hg19 (Hinxton)ENSG00000261475 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261475 [Gene_View]  chr16:31546698-31553567 [Contig_View]  LINC02190 [Vega]
ICGC DataPortalENSG00000261475
TCGA cBioPortalLINC02190
AceView (NCBI)LINC02190
Genatlas (Paris)LINC02190
WikiGenes105371173
SOURCE (Princeton)LINC02190
Genetics Home Reference (NIH)LINC02190
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02190  -     chr16:31546698-31553567 -  16p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02190  -     16p11.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02190 - 16p11.2 [CytoView hg19]  LINC02190 - 16p11.2 [CytoView hg38]
Mapping of homologs : NCBILINC02190 [Mapview hg19]  LINC02190 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02190
Alternative Splicing GalleryENSG00000261475
Gene ExpressionLINC02190 [ NCBI-GEO ]   LINC02190 [ EBI - ARRAY_EXPRESS ]   LINC02190 [ SEEK ]   LINC02190 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02190 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105371173
GTEX Portal (Tissue expression)LINC02190
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02190
DMDM Disease mutations105371173
Blocks (Seattle)LINC02190
Human Protein AtlasENSG00000261475
Protein Interaction databases
FunCoupENSG00000261475
BioGRIDLINC02190
STRING (EMBL)LINC02190
ZODIACLINC02190
Ontologies - Pathways
Huge Navigator LINC02190 [HugePedia]
snp3D : Map Gene to Disease105371173
BioCentury BCIQLINC02190
ClinGenLINC02190
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105371173
Clinical trialLINC02190
Miscellaneous
canSAR (ICR)LINC02190 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02190
EVEXLINC02190
GoPubMedLINC02190
iHOPLINC02190
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 : Mon Sep 18 13:16:01 CEST 2017

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