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LINC00278 (long intergenic non-protein coding RNA 278)

Identity

Alias_namesNCRNA00278
non-protein coding RNA 278
Other alias
HGNC (Hugo) LINC00278
LocusID (NCBI) 100873962
Atlas_Id 65342
Location Yp11.2  [Link to chromosome band Yp11]
Location_base_pair Starts at 3002996 and ends at 3102272 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)LINC00278   38712
Cards
Entrez_Gene (NCBI)LINC00278  100873962  long intergenic non-protein coding RNA 278
AliasesNCRNA00278
GeneCards (Weizmann)LINC00278
Ensembl hg19 (Hinxton)ENSG00000231535 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000231535 [Gene_View]  chrY:3002996-3102272 [Contig_View]  LINC00278 [Vega]
ICGC DataPortalENSG00000231535
TCGA cBioPortalLINC00278
AceView (NCBI)LINC00278
Genatlas (Paris)LINC00278
WikiGenes100873962
SOURCE (Princeton)LINC00278
Genetics Home Reference (NIH)LINC00278
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00278  -     chrY:3002996-3102272 +  Yp11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00278  -     Yp11.2   [Description]    (hg19-Feb_2009)
EnsemblLINC00278 - Yp11.2 [CytoView hg19]  LINC00278 - Yp11.2 [CytoView hg38]
Mapping of homologs : NCBILINC00278 [Mapview hg19]  LINC00278 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW772613 BF195971
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00278
Cluster EST : UnigeneHs.267256 [ NCBI ]
CGAP (NCI)Hs.267256
Alternative Splicing GalleryENSG00000231535
Gene ExpressionLINC00278 [ NCBI-GEO ]   LINC00278 [ EBI - ARRAY_EXPRESS ]   LINC00278 [ SEEK ]   LINC00278 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00278 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100873962
GTEX Portal (Tissue expression)LINC00278
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00278
DMDM Disease mutations100873962
Blocks (Seattle)LINC00278
Human Protein AtlasENSG00000231535
Protein Interaction databases
FunCoupENSG00000231535
BioGRIDLINC00278
STRING (EMBL)LINC00278
ZODIACLINC00278
Ontologies - Pathways
Huge Navigator LINC00278 [HugePedia]
snp3D : Map Gene to Disease100873962
BioCentury BCIQLINC00278
ClinGenLINC00278
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100873962
Clinical trialLINC00278
Miscellaneous
canSAR (ICR)LINC00278 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00278
EVEXLINC00278
GoPubMedLINC00278
iHOPLINC00278
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed Jun 7 15:56:10 CEST 2017

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