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LINC01752 (long intergenic non-protein coding RNA 1752)

Identity

Other alias-
HGNC (Hugo) LINC01752
LocusID (NCBI) 101929395
Atlas_Id 79964
Location 20p12.2  [Link to chromosome band 20p12]
Location_base_pair Starts at 10753090 and ends at 10754027 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)LINC01752   52540
Cards
Entrez_Gene (NCBI)LINC01752  101929395  long intergenic non-protein coding RNA 1752
Aliases
GeneCards (Weizmann)LINC01752
Ensembl hg19 (Hinxton)ENSG00000224961 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000224961 [Gene_View]  chr20:10753090-10754027 [Contig_View]  LINC01752 [Vega]
ICGC DataPortalENSG00000224961
TCGA cBioPortalLINC01752
AceView (NCBI)LINC01752
Genatlas (Paris)LINC01752
WikiGenes101929395
SOURCE (Princeton)LINC01752
Genetics Home Reference (NIH)LINC01752
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01752  -     chr20:10753090-10754027 +  20p12.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01752  -     20p12.2   [Description]    (hg19-Feb_2009)
EnsemblLINC01752 - 20p12.2 [CytoView hg19]  LINC01752 - 20p12.2 [CytoView hg38]
Mapping of homologs : NCBILINC01752 [Mapview hg19]  LINC01752 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BM987874
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01752
Cluster EST : UnigeneHs.244862 [ NCBI ]
CGAP (NCI)Hs.244862
Alternative Splicing GalleryENSG00000224961
Gene ExpressionLINC01752 [ NCBI-GEO ]   LINC01752 [ EBI - ARRAY_EXPRESS ]   LINC01752 [ SEEK ]   LINC01752 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01752 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929395
GTEX Portal (Tissue expression)LINC01752
Human Protein AtlasENSG00000224961-LINC01752 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01752
DMDM Disease mutations101929395
Blocks (Seattle)LINC01752
Human Protein Atlas [tissue]ENSG00000224961-LINC01752 [tissue]
Protein Interaction databases
FunCoupENSG00000224961
BioGRIDLINC01752
STRING (EMBL)LINC01752
ZODIACLINC01752
Ontologies - Pathways
Huge Navigator LINC01752 [HugePedia]
snp3D : Map Gene to Disease101929395
BioCentury BCIQLINC01752
ClinGenLINC01752
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929395
Clinical trialLINC01752
Miscellaneous
canSAR (ICR)LINC01752 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01752
EVEXLINC01752
GoPubMedLINC01752
iHOPLINC01752
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 : Tue Nov 21 13:41:49 CET 2017

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