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LINC02388 (long intergenic non-protein coding RNA 2388)

Identity

Other alias-
HGNC (Hugo) LINC02388
LocusID (NCBI) 101927653
Atlas_Id 79264
Location 12q14.1  [Link to chromosome band 12q14]
Location_base_pair Starts at 58565959 and ends at 58781716 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)LINC02388   53315
Cards
Entrez_Gene (NCBI)LINC02388  101927653  long intergenic non-protein coding RNA 2388
Aliases
GeneCards (Weizmann)LINC02388
Ensembl hg19 (Hinxton)ENSG00000257259 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000257259 [Gene_View]  chr12:58565959-58781716 [Contig_View]  LINC02388 [Vega]
ICGC DataPortalENSG00000257259
TCGA cBioPortalLINC02388
AceView (NCBI)LINC02388
Genatlas (Paris)LINC02388
WikiGenes101927653
SOURCE (Princeton)LINC02388
Genetics Home Reference (NIH)LINC02388
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02388  -     chr12:58565959-58781716 -  12q14.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02388  -     12q14.1   [Description]    (hg19-Feb_2009)
EnsemblLINC02388 - 12q14.1 [CytoView hg19]  LINC02388 - 12q14.1 [CytoView hg38]
Mapping of homologs : NCBILINC02388 [Mapview hg19]  LINC02388 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093124 BX109998 DB024932
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02388
Cluster EST : UnigeneHs.569099 [ NCBI ]
CGAP (NCI)Hs.569099
Alternative Splicing GalleryENSG00000257259
Gene ExpressionLINC02388 [ NCBI-GEO ]   LINC02388 [ EBI - ARRAY_EXPRESS ]   LINC02388 [ SEEK ]   LINC02388 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02388 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927653
GTEX Portal (Tissue expression)LINC02388
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02388
DMDM Disease mutations101927653
Blocks (Seattle)LINC02388
Human Protein AtlasENSG00000257259
Protein Interaction databases
FunCoupENSG00000257259
BioGRIDLINC02388
STRING (EMBL)LINC02388
ZODIACLINC02388
Ontologies - Pathways
Huge Navigator LINC02388 [HugePedia]
snp3D : Map Gene to Disease101927653
BioCentury BCIQLINC02388
ClinGenLINC02388
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927653
Clinical trialLINC02388
Miscellaneous
canSAR (ICR)LINC02388 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02388
EVEXLINC02388
GoPubMedLINC02388
iHOPLINC02388
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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