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LINC01568 (long intergenic non-protein coding RNA 1568)

Identity

Other alias-
HGNC (Hugo) LINC01568
LocusID (NCBI) 100506172
Atlas_Id 66103
Location 16q22.3  [Link to chromosome band 16q22]
Location_base_pair Starts at 73386805 and ends at 73421396 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)LINC01568   51371
Cards
Entrez_Gene (NCBI)LINC01568  100506172  long intergenic non-protein coding RNA 1568
Aliases
GeneCards (Weizmann)LINC01568
Ensembl hg19 (Hinxton)ENSG00000258779 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258779 [Gene_View]  chr16:73386805-73421396 [Contig_View]  LINC01568 [Vega]
ICGC DataPortalENSG00000258779
TCGA cBioPortalLINC01568
AceView (NCBI)LINC01568
Genatlas (Paris)LINC01568
WikiGenes100506172
SOURCE (Princeton)LINC01568
Genetics Home Reference (NIH)LINC01568
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01568  -     chr16:73386805-73421396 +  16q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01568  -     16q22.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01568 - 16q22.3 [CytoView hg19]  LINC01568 - 16q22.3 [CytoView hg38]
Mapping of homologs : NCBILINC01568 [Mapview hg19]  LINC01568 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC036646 BC042734
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01568
Cluster EST : UnigeneHs.637630 [ NCBI ]
CGAP (NCI)Hs.637630
Alternative Splicing GalleryENSG00000258779
Gene ExpressionLINC01568 [ NCBI-GEO ]   LINC01568 [ EBI - ARRAY_EXPRESS ]   LINC01568 [ SEEK ]   LINC01568 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01568 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506172
GTEX Portal (Tissue expression)LINC01568
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01568
DMDM Disease mutations100506172
Blocks (Seattle)LINC01568
Human Protein AtlasENSG00000258779
Protein Interaction databases
FunCoupENSG00000258779
BioGRIDLINC01568
STRING (EMBL)LINC01568
ZODIACLINC01568
Ontologies - Pathways
Huge Navigator LINC01568 [HugePedia]
snp3D : Map Gene to Disease100506172
BioCentury BCIQLINC01568
ClinGenLINC01568
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506172
Clinical trialLINC01568
Miscellaneous
canSAR (ICR)LINC01568 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01568
EVEXLINC01568
GoPubMedLINC01568
iHOPLINC01568
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 13:14:51 CEST 2017

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