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

LINC02439 (long intergenic non-protein coding RNA 2439)

Identity

Other alias-
HGNC (Hugo) LINC02439
LocusID (NCBI) 105370016
Atlas_Id 78852
Location 12q24.23  [Link to chromosome band 12q24]
Location_base_pair Starts at 118818806 and ends at 118833536 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)LINC02439   53371
Cards
Entrez_Gene (NCBI)LINC02439  105370016  long intergenic non-protein coding RNA 2439
Aliases
GeneCards (Weizmann)LINC02439
Ensembl hg19 (Hinxton)ENSG00000255814 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000255814 [Gene_View]  chr12:118818806-118833536 [Contig_View]  LINC02439 [Vega]
ICGC DataPortalENSG00000255814
TCGA cBioPortalLINC02439
AceView (NCBI)LINC02439
Genatlas (Paris)LINC02439
WikiGenes105370016
SOURCE (Princeton)LINC02439
Genetics Home Reference (NIH)LINC02439
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02439  -     chr12:118818806-118833536 -  12q24.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02439  -     12q24.23   [Description]    (hg19-Feb_2009)
EnsemblLINC02439 - 12q24.23 [CytoView hg19]  LINC02439 - 12q24.23 [CytoView hg38]
Mapping of homologs : NCBILINC02439 [Mapview hg19]  LINC02439 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA759109 AL037786
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02439
Cluster EST : UnigeneHs.550627 [ NCBI ]
CGAP (NCI)Hs.550627
Alternative Splicing GalleryENSG00000255814
Gene ExpressionLINC02439 [ NCBI-GEO ]   LINC02439 [ EBI - ARRAY_EXPRESS ]   LINC02439 [ SEEK ]   LINC02439 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02439 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105370016
GTEX Portal (Tissue expression)LINC02439
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02439
DMDM Disease mutations105370016
Blocks (Seattle)LINC02439
Human Protein AtlasENSG00000255814
Protein Interaction databases
FunCoupENSG00000255814
BioGRIDLINC02439
STRING (EMBL)LINC02439
ZODIACLINC02439
Ontologies - Pathways
Huge Navigator LINC02439 [HugePedia]
snp3D : Map Gene to Disease105370016
BioCentury BCIQLINC02439
ClinGenLINC02439
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105370016
Clinical trialLINC02439
Miscellaneous
canSAR (ICR)LINC02439 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02439
EVEXLINC02439
GoPubMedLINC02439
iHOPLINC02439
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 13:16:28 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.