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LINC02332 (long intergenic non-protein coding RNA 2332)

Identity

Other alias-
HGNC (Hugo) LINC02332
LocusID (NCBI) 105370400
Atlas_Id 79480
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 22556311 and ends at 22557062 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)LINC02332   53252
Cards
Entrez_Gene (NCBI)LINC02332  105370400  long intergenic non-protein coding RNA 2332
Aliases
GeneCards (Weizmann)LINC02332
Ensembl hg19 (Hinxton)ENSG00000259054 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000259054 [Gene_View]  chr14:22556311-22557062 [Contig_View]  LINC02332 [Vega]
ICGC DataPortalENSG00000259054
TCGA cBioPortalLINC02332
AceView (NCBI)LINC02332
Genatlas (Paris)LINC02332
WikiGenes105370400
SOURCE (Princeton)LINC02332
Genetics Home Reference (NIH)LINC02332
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02332  -     chr14:22556311-22557062 -  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02332  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02332 - 14q11.2 [CytoView hg19]  LINC02332 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBILINC02332 [Mapview hg19]  LINC02332 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02332
Alternative Splicing GalleryENSG00000259054
Gene ExpressionLINC02332 [ NCBI-GEO ]   LINC02332 [ EBI - ARRAY_EXPRESS ]   LINC02332 [ SEEK ]   LINC02332 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02332 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105370400
GTEX Portal (Tissue expression)LINC02332
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02332
DMDM Disease mutations105370400
Blocks (Seattle)LINC02332
Human Protein AtlasENSG00000259054
Protein Interaction databases
FunCoupENSG00000259054
BioGRIDLINC02332
STRING (EMBL)LINC02332
ZODIACLINC02332
Ontologies - Pathways
Huge Navigator LINC02332 [HugePedia]
snp3D : Map Gene to Disease105370400
BioCentury BCIQLINC02332
ClinGenLINC02332
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105370400
Clinical trialLINC02332
Miscellaneous
canSAR (ICR)LINC02332 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02332
EVEXLINC02332
GoPubMedLINC02332
iHOPLINC02332
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 13:16:16 CEST 2017

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