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LINC02297 (long intergenic non-protein coding RNA 2297)

Identity

Other alias-
HGNC (Hugo) LINC02297
LocusID (NCBI) 642426
Atlas_Id 80151
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 18630538 and ends at 18633634 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LINC02297   53214
Cards
Entrez_Gene (NCBI)LINC02297  642426  long intergenic non-protein coding RNA 2297
Aliases
GeneCards (Weizmann)LINC02297
Ensembl hg19 (Hinxton)ENSG00000257504 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000257504 [Gene_View]  chr14:18630538-18633634 [Contig_View]  LINC02297 [Vega]
ICGC DataPortalENSG00000257504
TCGA cBioPortalLINC02297
AceView (NCBI)LINC02297
Genatlas (Paris)LINC02297
WikiGenes642426
SOURCE (Princeton)LINC02297
Genetics Home Reference (NIH)LINC02297
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02297  -     chr14:18630538-18633634 -  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02297  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02297 - 14q11.2 [CytoView hg19]  LINC02297 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBILINC02297 [Mapview hg19]  LINC02297 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC015119
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02297
Cluster EST : UnigeneHs.578301 [ NCBI ]
CGAP (NCI)Hs.578301
Alternative Splicing GalleryENSG00000257504
Gene ExpressionLINC02297 [ NCBI-GEO ]   LINC02297 [ EBI - ARRAY_EXPRESS ]   LINC02297 [ SEEK ]   LINC02297 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02297 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)642426
GTEX Portal (Tissue expression)LINC02297
Human Protein AtlasENSG00000257504-LINC02297 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02297
DMDM Disease mutations642426
Blocks (Seattle)LINC02297
Human Protein Atlas [tissue]ENSG00000257504-LINC02297 [tissue]
Protein Interaction databases
FunCoupENSG00000257504
BioGRIDLINC02297
STRING (EMBL)LINC02297
ZODIACLINC02297
Ontologies - Pathways
Huge Navigator LINC02297 [HugePedia]
snp3D : Map Gene to Disease642426
BioCentury BCIQLINC02297
ClinGenLINC02297
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD642426
Clinical trialLINC02297
Miscellaneous
canSAR (ICR)LINC02297 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02297
EVEXLINC02297
GoPubMedLINC02297
iHOPLINC02297
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 : Tue Nov 21 13:29:51 CET 2017

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