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LINC02267 (long intergenic non-protein coding RNA 2267)

Identity

Other alias-
HGNC (Hugo) LINC02267
LocusID (NCBI) 105377338
Atlas_Id 79189
Location 4q22.3  [Link to chromosome band 4q22]
Location_base_pair Starts at 96310703 and ends at 96818415 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


External links

Nomenclature
HGNC (Hugo)LINC02267   53181
Cards
Entrez_Gene (NCBI)LINC02267  105377338  long intergenic non-protein coding RNA 2267
Aliases
GeneCards (Weizmann)LINC02267
Ensembl hg19 (Hinxton)ENSG00000248510 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000248510 [Gene_View]  ENSG00000248510 [Sequence]  chr4:96310703-96818415 [Contig_View]  LINC02267 [Vega]
ICGC DataPortalENSG00000248510
TCGA cBioPortalLINC02267
AceView (NCBI)LINC02267
Genatlas (Paris)LINC02267
WikiGenes105377338
SOURCE (Princeton)LINC02267
Genetics Home Reference (NIH)LINC02267
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02267  -     chr4:96310703-96818415 +  4q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02267  -     4q22.3   [Description]    (hg19-Feb_2009)
EnsemblLINC02267 - 4q22.3 [CytoView hg19]  LINC02267 - 4q22.3 [CytoView hg38]
Mapping of homologs : NCBILINC02267 [Mapview hg19]  LINC02267 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG527592 BX356497
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02267
Alternative Splicing GalleryENSG00000248510
Gene ExpressionLINC02267 [ NCBI-GEO ]   LINC02267 [ EBI - ARRAY_EXPRESS ]   LINC02267 [ SEEK ]   LINC02267 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02267 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105377338
GTEX Portal (Tissue expression)LINC02267
Human Protein AtlasENSG00000248510-LINC02267 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02267
DMDM Disease mutations105377338
Blocks (Seattle)LINC02267
Human Protein Atlas [tissue]ENSG00000248510-LINC02267 [tissue]
Protein Interaction databases
FunCoupENSG00000248510
BioGRIDLINC02267
STRING (EMBL)LINC02267
ZODIACLINC02267
Ontologies - Pathways
Huge Navigator LINC02267 [HugePedia]
snp3D : Map Gene to Disease105377338
BioCentury BCIQLINC02267
ClinGenLINC02267
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105377338
Clinical trialLINC02267
Miscellaneous
canSAR (ICR)LINC02267 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02267
EVEXLINC02267
GoPubMedLINC02267
iHOPLINC02267
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 Jul 30 13:57:23 CEST 2018

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