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LINC01087 (long intergenic non-protein coding RNA 1087)

Identity

Other alias-
HGNC (Hugo) LINC01087
LocusID (NCBI) 101927994
Atlas_Id 65773
Location 2q21.1  [Link to chromosome band 2q21]
Location_base_pair Starts at 131637025 and ends at 131649615 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)LINC01087   49144
Cards
Entrez_Gene (NCBI)LINC01087  101927994  long intergenic non-protein coding RNA 1087
Aliases
GeneCards (Weizmann)LINC01087
Ensembl hg19 (Hinxton)ENSG00000224559 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000224559 [Gene_View]  chr2:131637025-131649615 [Contig_View]  LINC01087 [Vega]
ICGC DataPortalENSG00000224559
TCGA cBioPortalLINC01087
AceView (NCBI)LINC01087
Genatlas (Paris)LINC01087
WikiGenes101927994
SOURCE (Princeton)LINC01087
Genetics Home Reference (NIH)LINC01087
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01087  -     chr2:131637025-131649615 +  2q21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01087  -     2q21.1   [Description]    (hg19-Feb_2009)
EnsemblLINC01087 - 2q21.1 [CytoView hg19]  LINC01087 - 2q21.1 [CytoView hg38]
Mapping of homologs : NCBILINC01087 [Mapview hg19]  LINC01087 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC036114
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01087
Cluster EST : UnigeneHs.635757 [ NCBI ]
CGAP (NCI)Hs.635757
Alternative Splicing GalleryENSG00000224559
Gene ExpressionLINC01087 [ NCBI-GEO ]   LINC01087 [ EBI - ARRAY_EXPRESS ]   LINC01087 [ SEEK ]   LINC01087 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01087 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927994
GTEX Portal (Tissue expression)LINC01087
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01087
DMDM Disease mutations101927994
Blocks (Seattle)LINC01087
Human Protein AtlasENSG00000224559
Protein Interaction databases
FunCoupENSG00000224559
BioGRIDLINC01087
STRING (EMBL)LINC01087
ZODIACLINC01087
Ontologies - Pathways
Huge Navigator LINC01087 [HugePedia]
snp3D : Map Gene to Disease101927994
BioCentury BCIQLINC01087
ClinGenLINC01087
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927994
Clinical trialLINC01087
Miscellaneous
canSAR (ICR)LINC01087 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01087
EVEXLINC01087
GoPubMedLINC01087
iHOPLINC01087
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 13:14:00 CEST 2017

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