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LINC02392 (long intergenic non-protein coding RNA 2392)

Identity

Other alias-
HGNC (Hugo) LINC02392
LocusID (NCBI) 105369893
Atlas_Id 79977
Location 12q21.33  [Link to chromosome band 12q21]
Location_base_pair Starts at 90293318 and ends at 90300698 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)LINC02392   53319
Cards
Entrez_Gene (NCBI)LINC02392  105369893  long intergenic non-protein coding RNA 2392
Aliases
GeneCards (Weizmann)LINC02392
Ensembl hg19 (Hinxton)ENSG00000258183 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258183 [Gene_View]  chr12:90293318-90300698 [Contig_View]  LINC02392 [Vega]
ICGC DataPortalENSG00000258183
TCGA cBioPortalLINC02392
AceView (NCBI)LINC02392
Genatlas (Paris)LINC02392
WikiGenes105369893
SOURCE (Princeton)LINC02392
Genetics Home Reference (NIH)LINC02392
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02392  -     chr12:90293318-90300698 +  12q21.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02392  -     12q21.33   [Description]    (hg19-Feb_2009)
EnsemblLINC02392 - 12q21.33 [CytoView hg19]  LINC02392 - 12q21.33 [CytoView hg38]
Mapping of homologs : NCBILINC02392 [Mapview hg19]  LINC02392 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DA887712 DB056805 DB057484
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02392
Cluster EST : UnigeneHs.577777 [ NCBI ]
CGAP (NCI)Hs.577777
Alternative Splicing GalleryENSG00000258183
Gene ExpressionLINC02392 [ NCBI-GEO ]   LINC02392 [ EBI - ARRAY_EXPRESS ]   LINC02392 [ SEEK ]   LINC02392 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02392 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105369893
GTEX Portal (Tissue expression)LINC02392
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02392
DMDM Disease mutations105369893
Blocks (Seattle)LINC02392
Human Protein AtlasENSG00000258183
Protein Interaction databases
FunCoupENSG00000258183
BioGRIDLINC02392
STRING (EMBL)LINC02392
ZODIACLINC02392
Ontologies - Pathways
Huge Navigator LINC02392 [HugePedia]
snp3D : Map Gene to Disease105369893
BioCentury BCIQLINC02392
ClinGenLINC02392
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105369893
Clinical trialLINC02392
Miscellaneous
canSAR (ICR)LINC02392 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02392
EVEXLINC02392
GoPubMedLINC02392
iHOPLINC02392
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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