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LINC00987 (long intergenic non-protein coding RNA 987)

Identity

Other alias-
HGNC (Hugo) LINC00987
LocusID (NCBI) 100499405
Atlas_Id 65714
Location 12p13.31  [Link to chromosome band 12p13]
Location_base_pair Starts at 9392599 and ends at 9395645 bp from pter ( according to hg19-Feb_2009)

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)LINC00987   48911
Cards
Entrez_Gene (NCBI)LINC00987  100499405  long intergenic non-protein coding RNA 987
Aliases
GeneCards (Weizmann)LINC00987
Ensembl hg19 (Hinxton)ENSG00000237248 [Gene_View]  chr12:9392599-9395645 [Contig_View]  LINC00987 [Vega]
Ensembl hg38 (Hinxton)ENSG00000237248 [Gene_View]  chr12:9392599-9395645 [Contig_View]  LINC00987 [Vega]
ICGC DataPortalENSG00000237248
TCGA cBioPortalLINC00987
AceView (NCBI)LINC00987
Genatlas (Paris)LINC00987
WikiGenes100499405
SOURCE (Princeton)LINC00987
Genetics Home Reference (NIH)LINC00987
Genomic and cartography
GoldenPath hg19 (UCSC)LINC00987  -     chr12:9392599-9395645 +  12p13.31   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LINC00987  -     12p13.31   [Description]    (hg38-Dec_2013)
EnsemblLINC00987 - 12p13.31 [CytoView hg19]  LINC00987 - 12p13.31 [CytoView hg38]
Mapping of homologs : NCBILINC00987 [Mapview hg19]  LINC00987 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK126248 HG504499
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000012 NC_018923 NT_009714 NW_004929383
Consensus coding sequences : CCDS (NCBI)LINC00987
Cluster EST : UnigeneHs.182314 [ NCBI ]
CGAP (NCI)Hs.182314
Alternative Splicing GalleryENSG00000237248
Gene ExpressionLINC00987 [ NCBI-GEO ]   LINC00987 [ EBI - ARRAY_EXPRESS ]   LINC00987 [ SEEK ]   LINC00987 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00987 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100499405
GTEX Portal (Tissue expression)LINC00987
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00987
DMDM Disease mutations100499405
Blocks (Seattle)LINC00987
Human Protein AtlasENSG00000237248
Protein Interaction databases
FunCoupENSG00000237248
BioGRIDLINC00987
STRING (EMBL)LINC00987
ZODIACLINC00987
Ontologies - Pathways
Huge Navigator LINC00987 [HugePedia]
snp3D : Map Gene to Disease100499405
BioCentury BCIQLINC00987
ClinGenLINC00987
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100499405
Clinical trialLINC00987
Miscellaneous
canSAR (ICR)LINC00987 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00987
EVEXLINC00987
GoPubMedLINC00987
iHOPLINC00987
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:12:46 CET 2017

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