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LINC00664 (long intergenic non-protein coding RNA 664)

Identity

Other alias-
HGNC (Hugo) LINC00664
LocusID (NCBI) 400680
Atlas_Id 65571
Location 19p12  [Link to chromosome band 19p12]
Location_base_pair Starts at 21483715 and ends at 21503238 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)LINC00664   44319
Cards
Entrez_Gene (NCBI)LINC00664  400680  long intergenic non-protein coding RNA 664
Aliases
GeneCards (Weizmann)LINC00664
Ensembl hg19 (Hinxton)ENSG00000268658 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000268658 [Gene_View]  chr19:21483715-21503238 [Contig_View]  LINC00664 [Vega]
ICGC DataPortalENSG00000268658
TCGA cBioPortalLINC00664
AceView (NCBI)LINC00664
Genatlas (Paris)LINC00664
WikiGenes400680
SOURCE (Princeton)LINC00664
Genetics Home Reference (NIH)LINC00664
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00664  -     chr19:21483715-21503238 +  19p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00664  -     19p12   [Description]    (hg19-Feb_2009)
EnsemblLINC00664 - 19p12 [CytoView hg19]  LINC00664 - 19p12 [CytoView hg38]
Mapping of homologs : NCBILINC00664 [Mapview hg19]  LINC00664 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK097381 BC040866 BX537835
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00664
Cluster EST : UnigeneHs.710554 [ NCBI ]
CGAP (NCI)Hs.710554
Alternative Splicing GalleryENSG00000268658
Gene ExpressionLINC00664 [ NCBI-GEO ]   LINC00664 [ EBI - ARRAY_EXPRESS ]   LINC00664 [ SEEK ]   LINC00664 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00664 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)400680
GTEX Portal (Tissue expression)LINC00664
Human Protein AtlasENSG00000268658-LINC00664 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00664
DMDM Disease mutations400680
Blocks (Seattle)LINC00664
Human Protein Atlas [tissue]ENSG00000268658-LINC00664 [tissue]
Protein Interaction databases
FunCoupENSG00000268658
BioGRIDLINC00664
STRING (EMBL)LINC00664
ZODIACLINC00664
Ontologies - Pathways
Huge Navigator LINC00664 [HugePedia]
snp3D : Map Gene to Disease400680
BioCentury BCIQLINC00664
ClinGenLINC00664
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD400680
Clinical trialLINC00664
Miscellaneous
canSAR (ICR)LINC00664 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00664
EVEXLINC00664
GoPubMedLINC00664
iHOPLINC00664
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 : Thu Nov 9 11:54:45 CET 2017

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