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LINC01766 (long intergenic non-protein coding RNA 1766)

Identity

Other alias-
HGNC (Hugo) LINC01766
LocusID (NCBI) 102723617
Atlas_Id 79961
Location 19q13.12  [Link to chromosome band 19q13]
Location_base_pair Starts at 35597895 and ends at 35601501 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)LINC01766   52556
Cards
Entrez_Gene (NCBI)LINC01766  102723617  long intergenic non-protein coding RNA 1766
Aliases
GeneCards (Weizmann)LINC01766
Ensembl hg19 (Hinxton)ENSG00000224910 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000224910 [Gene_View]  chr19:35597895-35601501 [Contig_View]  LINC01766 [Vega]
ICGC DataPortalENSG00000224910
TCGA cBioPortalLINC01766
AceView (NCBI)LINC01766
Genatlas (Paris)LINC01766
WikiGenes102723617
SOURCE (Princeton)LINC01766
Genetics Home Reference (NIH)LINC01766
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01766  -     chr19:35597895-35601501 +  19q13.12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01766  -     19q13.12   [Description]    (hg19-Feb_2009)
EnsemblLINC01766 - 19q13.12 [CytoView hg19]  LINC01766 - 19q13.12 [CytoView hg38]
Mapping of homologs : NCBILINC01766 [Mapview hg19]  LINC01766 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA913455
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01766
Cluster EST : UnigeneHs.579904 [ NCBI ]
CGAP (NCI)Hs.579904
Alternative Splicing GalleryENSG00000224910
Gene ExpressionLINC01766 [ NCBI-GEO ]   LINC01766 [ EBI - ARRAY_EXPRESS ]   LINC01766 [ SEEK ]   LINC01766 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01766 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102723617
GTEX Portal (Tissue expression)LINC01766
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01766
DMDM Disease mutations102723617
Blocks (Seattle)LINC01766
Human Protein AtlasENSG00000224910
Protein Interaction databases
FunCoupENSG00000224910
BioGRIDLINC01766
STRING (EMBL)LINC01766
ZODIACLINC01766
Ontologies - Pathways
Huge Navigator LINC01766 [HugePedia]
snp3D : Map Gene to Disease102723617
BioCentury BCIQLINC01766
ClinGenLINC01766
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102723617
Clinical trialLINC01766
Miscellaneous
canSAR (ICR)LINC01766 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01766
EVEXLINC01766
GoPubMedLINC01766
iHOPLINC01766
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 13:15:16 CEST 2017

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