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LINC00967 (long intergenic non-protein coding RNA 967)

Identity

Other alias-
HGNC (Hugo) LINC00967
LocusID (NCBI) 100505659
Atlas_Id 65706
Location 8q13.1  [Link to chromosome band 8q13]
Location_base_pair Starts at 67104349 and ends at 67109554 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)LINC00967   48725
Cards
Entrez_Gene (NCBI)LINC00967  100505659  long intergenic non-protein coding RNA 967
Aliases
GeneCards (Weizmann)LINC00967
Ensembl hg19 (Hinxton)ENSG00000253138 [Gene_View]  chr8:67104349-67109554 [Contig_View]  LINC00967 [Vega]
Ensembl hg38 (Hinxton)ENSG00000253138 [Gene_View]  chr8:67104349-67109554 [Contig_View]  LINC00967 [Vega]
ICGC DataPortalENSG00000253138
TCGA cBioPortalLINC00967
AceView (NCBI)LINC00967
Genatlas (Paris)LINC00967
WikiGenes100505659
SOURCE (Princeton)LINC00967
Genetics Home Reference (NIH)LINC00967
Genomic and cartography
GoldenPath hg19 (UCSC)LINC00967  -     chr8:67104349-67109554 +  8q13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LINC00967  -     8q13.1   [Description]    (hg38-Dec_2013)
EnsemblLINC00967 - 8q13.1 [CytoView hg19]  LINC00967 - 8q13.1 [CytoView hg38]
Mapping of homologs : NCBILINC00967 [Mapview hg19]  LINC00967 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX360434 BX389854 DB379123 HG501296 HG501297
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_008183 NW_004929339
Consensus coding sequences : CCDS (NCBI)LINC00967
Cluster EST : UnigeneHs.529729 [ NCBI ]
CGAP (NCI)Hs.529729
Alternative Splicing GalleryENSG00000253138
Gene ExpressionLINC00967 [ NCBI-GEO ]   LINC00967 [ EBI - ARRAY_EXPRESS ]   LINC00967 [ SEEK ]   LINC00967 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00967 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505659
GTEX Portal (Tissue expression)LINC00967
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00967
DMDM Disease mutations100505659
Blocks (Seattle)LINC00967
Human Protein AtlasENSG00000253138
Protein Interaction databases
FunCoupENSG00000253138
BioGRIDLINC00967
STRING (EMBL)LINC00967
ZODIACLINC00967
Ontologies - Pathways
Huge Navigator LINC00967 [HugePedia]
snp3D : Map Gene to Disease100505659
BioCentury BCIQLINC00967
ClinGenLINC00967
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505659
Clinical trialLINC00967
Miscellaneous
canSAR (ICR)LINC00967 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00967
EVEXLINC00967
GoPubMedLINC00967
iHOPLINC00967
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 12:12:45 CET 2017

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