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LINC02168 (long intergenic non-protein coding RNA 2168)

Identity

Other alias-
HGNC (Hugo) LINC02168
LocusID (NCBI) 105371252
Atlas_Id 79328
Location 16q12.1  [Link to chromosome band 16q12]
Location_base_pair Starts at 50806672 and ends at 50807629 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)LINC02168   53030
Cards
Entrez_Gene (NCBI)LINC02168  105371252  long intergenic non-protein coding RNA 2168
Aliases
GeneCards (Weizmann)LINC02168
Ensembl hg19 (Hinxton)ENSG00000261703 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261703 [Gene_View]  chr16:50806672-50807629 [Contig_View]  LINC02168 [Vega]
ICGC DataPortalENSG00000261703
TCGA cBioPortalLINC02168
AceView (NCBI)LINC02168
Genatlas (Paris)LINC02168
WikiGenes105371252
SOURCE (Princeton)LINC02168
Genetics Home Reference (NIH)LINC02168
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02168  -     chr16:50806672-50807629 +  16q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02168  -     16q12.1   [Description]    (hg19-Feb_2009)
EnsemblLINC02168 - 16q12.1 [CytoView hg19]  LINC02168 - 16q12.1 [CytoView hg38]
Mapping of homologs : NCBILINC02168 [Mapview hg19]  LINC02168 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02168
Alternative Splicing GalleryENSG00000261703
Gene ExpressionLINC02168 [ NCBI-GEO ]   LINC02168 [ EBI - ARRAY_EXPRESS ]   LINC02168 [ SEEK ]   LINC02168 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02168 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105371252
GTEX Portal (Tissue expression)LINC02168
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02168
DMDM Disease mutations105371252
Blocks (Seattle)LINC02168
Human Protein AtlasENSG00000261703
Protein Interaction databases
FunCoupENSG00000261703
BioGRIDLINC02168
STRING (EMBL)LINC02168
ZODIACLINC02168
Ontologies - Pathways
Huge Navigator LINC02168 [HugePedia]
snp3D : Map Gene to Disease105371252
BioCentury BCIQLINC02168
ClinGenLINC02168
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105371252
Clinical trialLINC02168
Miscellaneous
canSAR (ICR)LINC02168 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02168
EVEXLINC02168
GoPubMedLINC02168
iHOPLINC02168
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 13:15:58 CEST 2017

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