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LINC00665 (long intergenic non-protein coding RNA 665)

Identity

Other alias-
HGNC (Hugo) LINC00665
LocusID (NCBI) 100506930
Atlas_Id 65572
Location 19q13.12  [Link to chromosome band 19q13]
Location_base_pair Starts at 36319716 and ends at 36331718 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)LINC00665   44323
Cards
Entrez_Gene (NCBI)LINC00665  100506930  long intergenic non-protein coding RNA 665
Aliases
GeneCards (Weizmann)LINC00665
Ensembl hg19 (Hinxton)ENSG00000232677 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232677 [Gene_View]  chr19:36319716-36331718 [Contig_View]  LINC00665 [Vega]
ICGC DataPortalENSG00000232677
TCGA cBioPortalLINC00665
AceView (NCBI)LINC00665
Genatlas (Paris)LINC00665
WikiGenes100506930
SOURCE (Princeton)LINC00665
Genetics Home Reference (NIH)LINC00665
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00665  -     chr19:36319716-36331718 -  19q13.12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00665  -     19q13.12   [Description]    (hg19-Feb_2009)
EnsemblLINC00665 - 19q13.12 [CytoView hg19]  LINC00665 - 19q13.12 [CytoView hg38]
Mapping of homologs : NCBILINC00665 [Mapview hg19]  LINC00665 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI282277 AK090827 BC041949 BU071001
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00665
Cluster EST : UnigeneHs.595153 [ NCBI ]
CGAP (NCI)Hs.595153
Alternative Splicing GalleryENSG00000232677
Gene ExpressionLINC00665 [ NCBI-GEO ]   LINC00665 [ EBI - ARRAY_EXPRESS ]   LINC00665 [ SEEK ]   LINC00665 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00665 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506930
GTEX Portal (Tissue expression)LINC00665
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00665
DMDM Disease mutations100506930
Blocks (Seattle)LINC00665
Human Protein AtlasENSG00000232677
Protein Interaction databases
FunCoupENSG00000232677
BioGRIDLINC00665
STRING (EMBL)LINC00665
ZODIACLINC00665
Ontologies - Pathways
Huge Navigator LINC00665 [HugePedia]
snp3D : Map Gene to Disease100506930
BioCentury BCIQLINC00665
ClinGenLINC00665
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506930
Clinical trialLINC00665
Miscellaneous
canSAR (ICR)LINC00665 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00665
EVEXLINC00665
GoPubMedLINC00665
iHOPLINC00665
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 : Wed Jun 7 15:57:10 CEST 2017

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