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LINC01168 (long intergenic non-protein coding RNA 1168)

Identity

Other alias-
HGNC (Hugo) LINC01168
LocusID (NCBI) 399829
Atlas_Id 65833
Location 10q26.3  [Link to chromosome band 10q26]
Location_base_pair Starts at 132965534 and ends at 132976497 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LINC01168   49537
Cards
Entrez_Gene (NCBI)LINC01168  399829  long intergenic non-protein coding RNA 1168
Aliases
GeneCards (Weizmann)LINC01168
Ensembl hg19 (Hinxton)ENSG00000240707 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000240707 [Gene_View]  chr10:132965534-132976497 [Contig_View]  LINC01168 [Vega]
ICGC DataPortalENSG00000240707
TCGA cBioPortalLINC01168
AceView (NCBI)LINC01168
Genatlas (Paris)LINC01168
WikiGenes399829
SOURCE (Princeton)LINC01168
Genetics Home Reference (NIH)LINC01168
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01168  -     chr10:132965534-132976497 +  10q26.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01168  -     10q26.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01168 - 10q26.3 [CytoView hg19]  LINC01168 - 10q26.3 [CytoView hg38]
Mapping of homologs : NCBILINC01168 [Mapview hg19]  LINC01168 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK125849
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01168
Cluster EST : UnigeneHs.252872 [ NCBI ]
CGAP (NCI)Hs.252872
Alternative Splicing GalleryENSG00000240707
Gene ExpressionLINC01168 [ NCBI-GEO ]   LINC01168 [ EBI - ARRAY_EXPRESS ]   LINC01168 [ SEEK ]   LINC01168 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01168 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)399829
GTEX Portal (Tissue expression)LINC01168
Human Protein AtlasENSG00000240707-LINC01168 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01168
DMDM Disease mutations399829
Blocks (Seattle)LINC01168
Human Protein Atlas [tissue]ENSG00000240707-LINC01168 [tissue]
IPIIPI00930711   
Protein Interaction databases
FunCoupENSG00000240707
BioGRIDLINC01168
STRING (EMBL)LINC01168
ZODIACLINC01168
Ontologies - Pathways
Huge Navigator LINC01168 [HugePedia]
snp3D : Map Gene to Disease399829
BioCentury BCIQLINC01168
ClinGenLINC01168
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD399829
Clinical trialLINC01168
Miscellaneous
canSAR (ICR)LINC01168 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01168
EVEXLINC01168
GoPubMedLINC01168
iHOPLINC01168
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 : Tue Nov 21 13:21:55 CET 2017

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