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LINC01755 (long intergenic non-protein coding RNA 1755)

Identity

Other alias-
HGNC (Hugo) LINC01755
LocusID (NCBI) 105378738
Atlas_Id 78917
Location 1p32.2  [Link to chromosome band 1p32]
Location_base_pair Starts at 55945087 and ends at 55950119 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


External links

Nomenclature
HGNC (Hugo)LINC01755   52543
Cards
Entrez_Gene (NCBI)LINC01755  105378738  long intergenic non-protein coding RNA 1755
Aliases
GeneCards (Weizmann)LINC01755
Ensembl hg19 (Hinxton)ENSG00000233079 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233079 [Gene_View]  chr1:55945087-55950119 [Contig_View]  LINC01755 [Vega]
ICGC DataPortalENSG00000233079
TCGA cBioPortalLINC01755
AceView (NCBI)LINC01755
Genatlas (Paris)LINC01755
WikiGenes105378738
SOURCE (Princeton)LINC01755
Genetics Home Reference (NIH)LINC01755
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01755  -     chr1:55945087-55950119 +  1p32.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01755  -     1p32.2   [Description]    (hg19-Feb_2009)
EnsemblLINC01755 - 1p32.2 [CytoView hg19]  LINC01755 - 1p32.2 [CytoView hg38]
Mapping of homologs : NCBILINC01755 [Mapview hg19]  LINC01755 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX104945
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01755
Cluster EST : UnigeneHs.121473 [ NCBI ]
CGAP (NCI)Hs.121473
Alternative Splicing GalleryENSG00000233079
Gene ExpressionLINC01755 [ NCBI-GEO ]   LINC01755 [ EBI - ARRAY_EXPRESS ]   LINC01755 [ SEEK ]   LINC01755 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01755 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105378738
GTEX Portal (Tissue expression)LINC01755
Human Protein AtlasENSG00000233079-LINC01755 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01755
DMDM Disease mutations105378738
Blocks (Seattle)LINC01755
Human Protein Atlas [tissue]ENSG00000233079-LINC01755 [tissue]
Protein Interaction databases
FunCoupENSG00000233079
BioGRIDLINC01755
STRING (EMBL)LINC01755
ZODIACLINC01755
Ontologies - Pathways
Huge Navigator LINC01755 [HugePedia]
snp3D : Map Gene to Disease105378738
BioCentury BCIQLINC01755
ClinGenLINC01755
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105378738
Clinical trialLINC01755
Miscellaneous
canSAR (ICR)LINC01755 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01755
EVEXLINC01755
GoPubMedLINC01755
iHOPLINC01755
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 13:01:11 CET 2017

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