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LINC01690 (long intergenic non-protein coding RNA 1690)

Identity

Other alias-
HGNC (Hugo) LINC01690
LocusID (NCBI) 102724502
Atlas_Id 79317
Location 21q22.11  [Link to chromosome band 21q22]
Location_base_pair Starts at 32958888 and ends at 32960564 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


External links

Nomenclature
HGNC (Hugo)LINC01690   52477
Cards
Entrez_Gene (NCBI)LINC01690  102724502  long intergenic non-protein coding RNA 1690
Aliases
GeneCards (Weizmann)LINC01690
Ensembl hg19 (Hinxton)ENSG00000228961 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000228961 [Gene_View]  chr21:32958888-32960564 [Contig_View]  LINC01690 [Vega]
ICGC DataPortalENSG00000228961
TCGA cBioPortalLINC01690
AceView (NCBI)LINC01690
Genatlas (Paris)LINC01690
WikiGenes102724502
SOURCE (Princeton)LINC01690
Genetics Home Reference (NIH)LINC01690
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01690  -     chr21:32958888-32960564 +  21q22.11   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01690  -     21q22.11   [Description]    (hg19-Feb_2009)
EnsemblLINC01690 - 21q22.11 [CytoView hg19]  LINC01690 - 21q22.11 [CytoView hg38]
Mapping of homologs : NCBILINC01690 [Mapview hg19]  LINC01690 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX095520
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01690
Cluster EST : UnigeneHs.130572 [ NCBI ]
CGAP (NCI)Hs.130572
Alternative Splicing GalleryENSG00000228961
Gene ExpressionLINC01690 [ NCBI-GEO ]   LINC01690 [ EBI - ARRAY_EXPRESS ]   LINC01690 [ SEEK ]   LINC01690 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01690 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102724502
GTEX Portal (Tissue expression)LINC01690
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01690
DMDM Disease mutations102724502
Blocks (Seattle)LINC01690
Human Protein AtlasENSG00000228961
Protein Interaction databases
FunCoupENSG00000228961
BioGRIDLINC01690
STRING (EMBL)LINC01690
ZODIACLINC01690
Ontologies - Pathways
Huge Navigator LINC01690 [HugePedia]
snp3D : Map Gene to Disease102724502
BioCentury BCIQLINC01690
ClinGenLINC01690
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102724502
Clinical trialLINC01690
Miscellaneous
canSAR (ICR)LINC01690 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01690
EVEXLINC01690
GoPubMedLINC01690
iHOPLINC01690
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:15:06 CEST 2017

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