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LINC01487 (long intergenic non-protein coding RNA 1487)

Identity

Other alias-
HGNC (Hugo) LINC01487
LocusID (NCBI) 101928190
Atlas_Id 66029
Location 3q25.2  [Link to chromosome band 3q25]
Location_base_pair Starts at 155240945 and ends at 155243123 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)LINC01487   51139
Cards
Entrez_Gene (NCBI)LINC01487  101928190  long intergenic non-protein coding RNA 1487
Aliases
GeneCards (Weizmann)LINC01487
Ensembl hg19 (Hinxton)ENSG00000241336 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000241336 [Gene_View]  chr3:155240945-155243123 [Contig_View]  LINC01487 [Vega]
ICGC DataPortalENSG00000241336
TCGA cBioPortalLINC01487
AceView (NCBI)LINC01487
Genatlas (Paris)LINC01487
WikiGenes101928190
SOURCE (Princeton)LINC01487
Genetics Home Reference (NIH)LINC01487
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01487  -     chr3:155240945-155243123 +  3q25.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01487  -     3q25.2   [Description]    (hg19-Feb_2009)
EnsemblLINC01487 - 3q25.2 [CytoView hg19]  LINC01487 - 3q25.2 [CytoView hg38]
Mapping of homologs : NCBILINC01487 [Mapview hg19]  LINC01487 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC037382 BG772196 BU570602
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01487
Cluster EST : UnigeneHs.121410 [ NCBI ]
CGAP (NCI)Hs.121410
Alternative Splicing GalleryENSG00000241336
Gene ExpressionLINC01487 [ NCBI-GEO ]   LINC01487 [ EBI - ARRAY_EXPRESS ]   LINC01487 [ SEEK ]   LINC01487 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01487 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928190
GTEX Portal (Tissue expression)LINC01487
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01487
DMDM Disease mutations101928190
Blocks (Seattle)LINC01487
Human Protein AtlasENSG00000241336
Protein Interaction databases
FunCoupENSG00000241336
BioGRIDLINC01487
STRING (EMBL)LINC01487
ZODIACLINC01487
Ontologies - Pathways
Huge Navigator LINC01487 [HugePedia]
snp3D : Map Gene to Disease101928190
BioCentury BCIQLINC01487
ClinGenLINC01487
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928190
Clinical trialLINC01487
Miscellaneous
canSAR (ICR)LINC01487 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01487
EVEXLINC01487
GoPubMedLINC01487
iHOPLINC01487
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 : Fri May 19 11:22:56 CEST 2017

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