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LINC02389 (long intergenic non-protein coding RNA 2389)

Identity

Alias_symbol (synonym)FLJ41278
Other alias-
HGNC (Hugo) LINC02389
LocusID (NCBI) 400046
Atlas_Id 80131
Location 12q14.3  [Link to chromosome band 12q14]
Location_base_pair Starts at 64883774 and ends at 64977522 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)LINC02389   53316
Cards
Entrez_Gene (NCBI)LINC02389  400046  long intergenic non-protein coding RNA 2389
Aliases
GeneCards (Weizmann)LINC02389
Ensembl hg19 (Hinxton)ENSG00000255693 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000255693 [Gene_View]  chr12:64883774-64977522 [Contig_View]  LINC02389 [Vega]
ICGC DataPortalENSG00000255693
TCGA cBioPortalLINC02389
AceView (NCBI)LINC02389
Genatlas (Paris)LINC02389
WikiGenes400046
SOURCE (Princeton)LINC02389
Genetics Home Reference (NIH)LINC02389
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02389  -     chr12:64883774-64977522 +  12q14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02389  -     12q14.3   [Description]    (hg19-Feb_2009)
EnsemblLINC02389 - 12q14.3 [CytoView hg19]  LINC02389 - 12q14.3 [CytoView hg38]
Mapping of homologs : NCBILINC02389 [Mapview hg19]  LINC02389 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123272 BU782746
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02389
Cluster EST : UnigeneHs.591032 [ NCBI ]
CGAP (NCI)Hs.591032
Alternative Splicing GalleryENSG00000255693
Gene ExpressionLINC02389 [ NCBI-GEO ]   LINC02389 [ EBI - ARRAY_EXPRESS ]   LINC02389 [ SEEK ]   LINC02389 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02389 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)400046
GTEX Portal (Tissue expression)LINC02389
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02389
DMDM Disease mutations400046
Blocks (Seattle)LINC02389
Human Protein AtlasENSG00000255693
Protein Interaction databases
FunCoupENSG00000255693
BioGRIDLINC02389
STRING (EMBL)LINC02389
ZODIACLINC02389
Ontologies - Pathways
Huge Navigator LINC02389 [HugePedia]
snp3D : Map Gene to Disease400046
BioCentury BCIQLINC02389
ClinGenLINC02389
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD400046
Clinical trialLINC02389
Miscellaneous
canSAR (ICR)LINC02389 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02389
EVEXLINC02389
GoPubMedLINC02389
iHOPLINC02389
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 : Mon Sep 18 13:16:23 CEST 2017

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