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LINC01761 (long intergenic non-protein coding RNA 1761)

Identity

Other alias-
HGNC (Hugo) LINC01761
LocusID (NCBI) 440594
Atlas_Id 79114
Location 1p21.3  [Link to chromosome band 1p21]
Location_base_pair Starts at 95474737 and ends at 95479356 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)LINC01761   52551
Cards
Entrez_Gene (NCBI)LINC01761  440594  long intergenic non-protein coding RNA 1761
Aliases
GeneCards (Weizmann)LINC01761
Ensembl hg19 (Hinxton)ENSG00000233907 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233907 [Gene_View]  chr1:95474737-95479356 [Contig_View]  LINC01761 [Vega]
ICGC DataPortalENSG00000233907
TCGA cBioPortalLINC01761
AceView (NCBI)LINC01761
Genatlas (Paris)LINC01761
WikiGenes440594
SOURCE (Princeton)LINC01761
Genetics Home Reference (NIH)LINC01761
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01761  -     chr1:95474737-95479356 +  1p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01761  -     1p21.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01761 - 1p21.3 [CytoView hg19]  LINC01761 - 1p21.3 [CytoView hg38]
Mapping of homologs : NCBILINC01761 [Mapview hg19]  LINC01761 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK056224
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01761
Cluster EST : UnigeneHs.514123 [ NCBI ]
CGAP (NCI)Hs.514123
Alternative Splicing GalleryENSG00000233907
Gene ExpressionLINC01761 [ NCBI-GEO ]   LINC01761 [ EBI - ARRAY_EXPRESS ]   LINC01761 [ SEEK ]   LINC01761 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01761 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)440594
GTEX Portal (Tissue expression)LINC01761
Human Protein AtlasENSG00000233907-LINC01761 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01761
DMDM Disease mutations440594
Blocks (Seattle)LINC01761
Human Protein Atlas [tissue]ENSG00000233907-LINC01761 [tissue]
Protein Interaction databases
FunCoupENSG00000233907
BioGRIDLINC01761
STRING (EMBL)LINC01761
ZODIACLINC01761
Ontologies - Pathways
Huge Navigator LINC01761 [HugePedia]
snp3D : Map Gene to Disease440594
BioCentury BCIQLINC01761
ClinGenLINC01761
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD440594
Clinical trialLINC01761
Miscellaneous
canSAR (ICR)LINC01761 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01761
EVEXLINC01761
GoPubMedLINC01761
iHOPLINC01761
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Nov 20 19:40:07 CET 2017

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