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LINC02387 (long intergenic non-protein coding RNA 2387)

Identity

Other alias-
HGNC (Hugo) LINC02387
LocusID (NCBI) 101929027
Atlas_Id 79115
Location 12p11.21  [Link to chromosome band 12p11]
Location_base_pair Starts at 31363481 and ends at 31369301 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)LINC02387   53313
Cards
Entrez_Gene (NCBI)LINC02387  101929027  long intergenic non-protein coding RNA 2387
Aliases
GeneCards (Weizmann)LINC02387
Ensembl hg19 (Hinxton)ENSG00000256232 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000256232 [Gene_View]  chr12:31363481-31369301 [Contig_View]  LINC02387 [Vega]
ICGC DataPortalENSG00000256232
TCGA cBioPortalLINC02387
AceView (NCBI)LINC02387
Genatlas (Paris)LINC02387
WikiGenes101929027
SOURCE (Princeton)LINC02387
Genetics Home Reference (NIH)LINC02387
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02387  -     chr12:31363481-31369301 -  12p11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02387  -     12p11.21   [Description]    (hg19-Feb_2009)
EnsemblLINC02387 - 12p1121 [ytmView hg19]  LINC02387 - 12p11.21 [CytoView hg38]
Mapping of homologs : NCBILINC02387 [Mapview hg19]  LINC02387 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC039477 BM459911 CB106476
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02387
Cluster EST : UnigeneHs.609199 [ NCBI ]
CGAP (NCI)Hs.609199
Alternative Splicing GalleryENSG00000256232
Gene ExpressionLINC02387 [ NCBI-GEO ]   LINC02387 [ EBI - ARRAY_EXPRESS ]   LINC02387 [ SEEK ]   LINC02387 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02387 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929027
GTEX Portal (Tissue expression)LINC02387
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02387
DMDM Disease mutations101929027
Blocks (Seattle)LINC02387
Human Protein AtlasENSG00000256232
Protein Interaction databases
FunCoupENSG00000256232
BioGRIDLINC02387
STRING (EMBL)LINC02387
ZODIACLINC02387
Ontologies - Pathways
Huge Navigator LINC02387 [HugePedia]
snp3D : Map Gene to Disease101929027
BioCentury BCIQLINC02387
ClinGenLINC02387
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929027
Clinical trialLINC02387
Miscellaneous
canSAR (ICR)LINC02387 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02387
EVEXLINC02387
GoPubMedLINC02387
iHOPLINC02387
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 : Mon Sep 18 13:16:22 CEST 2017

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