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LINC02178 (long intergenic non-protein coding RNA 2178)

Identity

Other alias-
HGNC (Hugo) LINC02178
LocusID (NCBI) 105371248
Atlas_Id 79852
Location 16q12.1  [Link to chromosome band 16q12]
Location_base_pair Starts at 50390916 and ends at 50395133 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)LINC02178   53040
Cards
Entrez_Gene (NCBI)LINC02178  105371248  long intergenic non-protein coding RNA 2178
Aliases
GeneCards (Weizmann)LINC02178
Ensembl hg19 (Hinxton)ENSG00000261092 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261092 [Gene_View]  chr16:50390916-50395133 [Contig_View]  LINC02178 [Vega]
ICGC DataPortalENSG00000261092
TCGA cBioPortalLINC02178
AceView (NCBI)LINC02178
Genatlas (Paris)LINC02178
WikiGenes105371248
SOURCE (Princeton)LINC02178
Genetics Home Reference (NIH)LINC02178
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02178  -     chr16:50390916-50395133 -  16q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02178  -     16q12.1   [Description]    (hg19-Feb_2009)
EnsemblLINC02178 - 16q12.1 [CytoView hg19]  LINC02178 - 16q12.1 [CytoView hg38]
Mapping of homologs : NCBILINC02178 [Mapview hg19]  LINC02178 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02178
Alternative Splicing GalleryENSG00000261092
Gene ExpressionLINC02178 [ NCBI-GEO ]   LINC02178 [ EBI - ARRAY_EXPRESS ]   LINC02178 [ SEEK ]   LINC02178 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02178 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105371248
GTEX Portal (Tissue expression)LINC02178
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02178
DMDM Disease mutations105371248
Blocks (Seattle)LINC02178
Human Protein AtlasENSG00000261092
Protein Interaction databases
FunCoupENSG00000261092
BioGRIDLINC02178
STRING (EMBL)LINC02178
ZODIACLINC02178
Ontologies - Pathways
Huge Navigator LINC02178 [HugePedia]
snp3D : Map Gene to Disease105371248
BioCentury BCIQLINC02178
ClinGenLINC02178
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105371248
Clinical trialLINC02178
Miscellaneous
canSAR (ICR)LINC02178 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02178
EVEXLINC02178
GoPubMedLINC02178
iHOPLINC02178
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 : Mon Sep 18 13:15:59 CEST 2017

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