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LINC01569 (long intergenic non-protein coding RNA 1569)

Identity

Alias_symbol (synonym)TCONS_00024567
Other alias-
HGNC (Hugo) LINC01569
LocusID (NCBI) 100507501
Atlas_Id 66104
Location 16p13.3  [Link to chromosome band 16p13]
Location_base_pair Starts at 4245825 and ends at 4253789 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)LINC01569   51380
Cards
Entrez_Gene (NCBI)LINC01569  100507501  long intergenic non-protein coding RNA 1569
Aliases
GeneCards (Weizmann)LINC01569
Ensembl hg19 (Hinxton)ENSG00000262468 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000262468 [Gene_View]  chr16:4245825-4253789 [Contig_View]  LINC01569 [Vega]
ICGC DataPortalENSG00000262468
TCGA cBioPortalLINC01569
AceView (NCBI)LINC01569
Genatlas (Paris)LINC01569
WikiGenes100507501
SOURCE (Princeton)LINC01569
Genetics Home Reference (NIH)LINC01569
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01569  -     chr16:4245825-4253789 -  16p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01569  -     16p13.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01569 - 16p13.3 [CytoView hg19]  LINC01569 - 16p13.3 [CytoView hg38]
Mapping of homologs : NCBILINC01569 [Mapview hg19]  LINC01569 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK094828
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01569
Cluster EST : UnigeneHs.632979 [ NCBI ]
CGAP (NCI)Hs.632979
Alternative Splicing GalleryENSG00000262468
Gene ExpressionLINC01569 [ NCBI-GEO ]   LINC01569 [ EBI - ARRAY_EXPRESS ]   LINC01569 [ SEEK ]   LINC01569 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01569 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507501
GTEX Portal (Tissue expression)LINC01569
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01569
DMDM Disease mutations100507501
Blocks (Seattle)LINC01569
Human Protein AtlasENSG00000262468
Protein Interaction databases
FunCoupENSG00000262468
BioGRIDLINC01569
STRING (EMBL)LINC01569
ZODIACLINC01569
Ontologies - Pathways
Huge Navigator LINC01569 [HugePedia]
snp3D : Map Gene to Disease100507501
BioCentury BCIQLINC01569
ClinGenLINC01569
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507501
Clinical trialLINC01569
Miscellaneous
canSAR (ICR)LINC01569 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01569
EVEXLINC01569
GoPubMedLINC01569
iHOPLINC01569
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 13:14:51 CEST 2017

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