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

LINC02189 (long intergenic non-protein coding RNA 2189)

Identity

Other alias-
HGNC (Hugo) LINC02189
LocusID (NCBI) 101928614
Atlas_Id 79503
Location 16q24.1  [Link to chromosome band 16q24]
Location_base_pair Starts at 86720684 and ends at 86721959 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)LINC02189   53051
Cards
Entrez_Gene (NCBI)LINC02189  101928614  long intergenic non-protein coding RNA 2189
Aliases
GeneCards (Weizmann)LINC02189
Ensembl hg19 (Hinxton)ENSG00000260026 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000260026 [Gene_View]  chr16:86720684-86721959 [Contig_View]  LINC02189 [Vega]
ICGC DataPortalENSG00000260026
TCGA cBioPortalLINC02189
AceView (NCBI)LINC02189
Genatlas (Paris)LINC02189
WikiGenes101928614
SOURCE (Princeton)LINC02189
Genetics Home Reference (NIH)LINC02189
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02189  -     chr16:86720684-86721959 -  16q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02189  -     16q24.1   [Description]    (hg19-Feb_2009)
EnsemblLINC02189 - 16q24.1 [CytoView hg19]  LINC02189 - 16q24.1 [CytoView hg38]
Mapping of homologs : NCBILINC02189 [Mapview hg19]  LINC02189 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI207158 BC041439 BC062224
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02189
Cluster EST : UnigeneHs.399823 [ NCBI ]
CGAP (NCI)Hs.399823
Alternative Splicing GalleryENSG00000260026
Gene ExpressionLINC02189 [ NCBI-GEO ]   LINC02189 [ EBI - ARRAY_EXPRESS ]   LINC02189 [ SEEK ]   LINC02189 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02189 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928614
GTEX Portal (Tissue expression)LINC02189
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02189
DMDM Disease mutations101928614
Blocks (Seattle)LINC02189
Human Protein AtlasENSG00000260026
Protein Interaction databases
FunCoupENSG00000260026
BioGRIDLINC02189
STRING (EMBL)LINC02189
ZODIACLINC02189
Ontologies - Pathways
Huge Navigator LINC02189 [HugePedia]
snp3D : Map Gene to Disease101928614
BioCentury BCIQLINC02189
ClinGenLINC02189
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928614
Clinical trialLINC02189
Miscellaneous
canSAR (ICR)LINC02189 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02189
EVEXLINC02189
GoPubMedLINC02189
iHOPLINC02189
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 13:16:00 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.