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LINC02322 (long intergenic non-protein coding RNA 2322)

Identity

Other alias-
HGNC (Hugo) LINC02322
LocusID (NCBI) 101927729
Atlas_Id 79588
Location 14q23.1  [Link to chromosome band 14q23]
Location_base_pair Starts at 60323196 and ends at 60323907 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)LINC02322   53241
Cards
Entrez_Gene (NCBI)LINC02322  101927729  long intergenic non-protein coding RNA 2322
Aliases
GeneCards (Weizmann)LINC02322
Ensembl hg19 (Hinxton)ENSG00000258556 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258556 [Gene_View]  chr14:60323196-60323907 [Contig_View]  LINC02322 [Vega]
ICGC DataPortalENSG00000258556
TCGA cBioPortalLINC02322
AceView (NCBI)LINC02322
Genatlas (Paris)LINC02322
WikiGenes101927729
SOURCE (Princeton)LINC02322
Genetics Home Reference (NIH)LINC02322
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02322  -     chr14:60323196-60323907 +  14q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02322  -     14q23.1   [Description]    (hg19-Feb_2009)
EnsemblLINC02322 - 14q23.1 [CytoView hg19]  LINC02322 - 14q23.1 [CytoView hg38]
Mapping of homologs : NCBILINC02322 [Mapview hg19]  LINC02322 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02322
Alternative Splicing GalleryENSG00000258556
Gene ExpressionLINC02322 [ NCBI-GEO ]   LINC02322 [ EBI - ARRAY_EXPRESS ]   LINC02322 [ SEEK ]   LINC02322 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02322 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927729
GTEX Portal (Tissue expression)LINC02322
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02322
DMDM Disease mutations101927729
Blocks (Seattle)LINC02322
Human Protein AtlasENSG00000258556
Protein Interaction databases
FunCoupENSG00000258556
BioGRIDLINC02322
STRING (EMBL)LINC02322
ZODIACLINC02322
Ontologies - Pathways
Huge Navigator LINC02322 [HugePedia]
snp3D : Map Gene to Disease101927729
BioCentury BCIQLINC02322
ClinGenLINC02322
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927729
Clinical trialLINC02322
Miscellaneous
canSAR (ICR)LINC02322 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02322
EVEXLINC02322
GoPubMedLINC02322
iHOPLINC02322
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:16:15 CEST 2017

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