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LINC02299 (long intergenic non-protein coding RNA 2299)

Identity

Other alias-
HGNC (Hugo) LINC02299
LocusID (NCBI) 105370646
Atlas_Id 79562
Location 14q32.2  [Link to chromosome band 14q32]
Location_base_pair Starts at 96741191 and ends at 96790613 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)LINC02299   53218
Cards
Entrez_Gene (NCBI)LINC02299  105370646  long intergenic non-protein coding RNA 2299
Aliases
GeneCards (Weizmann)LINC02299
Ensembl hg19 (Hinxton)ENSG00000258979 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258979 [Gene_View]  chr14:96741191-96790613 [Contig_View]  LINC02299 [Vega]
ICGC DataPortalENSG00000258979
TCGA cBioPortalLINC02299
AceView (NCBI)LINC02299
Genatlas (Paris)LINC02299
WikiGenes105370646
SOURCE (Princeton)LINC02299
Genetics Home Reference (NIH)LINC02299
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02299  -     chr14:96741191-96790613 +  14q32.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02299  -     14q32.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02299 - 14q32.2 [CytoView hg19]  LINC02299 - 14q32.2 [CytoView hg38]
Mapping of homologs : NCBILINC02299 [Mapview hg19]  LINC02299 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02299
Alternative Splicing GalleryENSG00000258979
Gene ExpressionLINC02299 [ NCBI-GEO ]   LINC02299 [ EBI - ARRAY_EXPRESS ]   LINC02299 [ SEEK ]   LINC02299 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02299 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105370646
GTEX Portal (Tissue expression)LINC02299
Human Protein AtlasENSG00000258979-LINC02299 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02299
DMDM Disease mutations105370646
Blocks (Seattle)LINC02299
Human Protein Atlas [tissue]ENSG00000258979-LINC02299 [tissue]
Protein Interaction databases
FunCoupENSG00000258979
BioGRIDLINC02299
STRING (EMBL)LINC02299
ZODIACLINC02299
Ontologies - Pathways
Huge Navigator LINC02299 [HugePedia]
snp3D : Map Gene to Disease105370646
BioCentury BCIQLINC02299
ClinGenLINC02299
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105370646
Clinical trialLINC02299
Miscellaneous
canSAR (ICR)LINC02299 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02299
EVEXLINC02299
GoPubMedLINC02299
iHOPLINC02299
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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