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LINC01176 (long intergenic non-protein coding RNA 1176)

Identity

Other alias-
HGNC (Hugo) LINC01176
LocusID (NCBI) 100506516
Atlas_Id 65836
Location 7p14.3  [Link to chromosome band 7p14]
Location_base_pair Starts at 30430501 and ends at 30443670 bp from pter ( according to hg19-Feb_2009)

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)LINC01176   49548
Cards
Entrez_Gene (NCBI)LINC01176  100506516  long intergenic non-protein coding RNA 1176
Aliases
GeneCards (Weizmann)LINC01176
Ensembl hg19 (Hinxton)ENSG00000281404 [Gene_View]  chr7:30430501-30443670 [Contig_View]  LINC01176 [Vega]
Ensembl hg38 (Hinxton)ENSG00000281404 [Gene_View]  chr7:30430501-30443670 [Contig_View]  LINC01176 [Vega]
ICGC DataPortalENSG00000281404
TCGA cBioPortalLINC01176
AceView (NCBI)LINC01176
Genatlas (Paris)LINC01176
WikiGenes100506516
SOURCE (Princeton)LINC01176
Genetics Home Reference (NIH)LINC01176
Genomic and cartography
GoldenPath hg19 (UCSC)LINC01176  -     chr7:30430501-30443670 +  7p14.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LINC01176  -     7p14.3   [Description]    (hg38-Dec_2013)
EnsemblLINC01176 - 7p14.3 [CytoView hg19]  LINC01176 - 7p14.3 [CytoView hg38]
Mapping of homologs : NCBILINC01176 [Mapview hg19]  LINC01176 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BM981427
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000007 NC_018918 NT_007819 NW_004929329
Consensus coding sequences : CCDS (NCBI)LINC01176
Alternative Splicing GalleryENSG00000281404
Gene ExpressionLINC01176 [ NCBI-GEO ]   LINC01176 [ EBI - ARRAY_EXPRESS ]   LINC01176 [ SEEK ]   LINC01176 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01176 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506516
GTEX Portal (Tissue expression)LINC01176
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01176
DMDM Disease mutations100506516
Blocks (Seattle)LINC01176
Human Protein AtlasENSG00000281404
Protein Interaction databases
FunCoupENSG00000281404
BioGRIDLINC01176
STRING (EMBL)LINC01176
ZODIACLINC01176
Ontologies - Pathways
Huge Navigator LINC01176 [HugePedia]
snp3D : Map Gene to Disease100506516
BioCentury BCIQLINC01176
ClinGenLINC01176
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506516
Clinical trialLINC01176
Miscellaneous
canSAR (ICR)LINC01176 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01176
EVEXLINC01176
GoPubMedLINC01176
iHOPLINC01176
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 Mar 14 12:13:16 CET 2017

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