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LINC00637 (long intergenic non-protein coding RNA 637)

Identity

Other alias-
HGNC (Hugo) LINC00637
LocusID (NCBI) 145216
Atlas_Id 65552
Location 14q32.33  [Link to chromosome band 14q32]
Location_base_pair Starts at 103847721 and ends at 103858049 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)LINC00637   27069
Cards
Entrez_Gene (NCBI)LINC00637  145216  long intergenic non-protein coding RNA 637
Aliases
GeneCards (Weizmann)LINC00637
Ensembl hg19 (Hinxton)ENSG00000258735 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258735 [Gene_View]  chr14:103847721-103858049 [Contig_View]  LINC00637 [Vega]
ICGC DataPortalENSG00000258735
TCGA cBioPortalLINC00637
AceView (NCBI)LINC00637
Genatlas (Paris)LINC00637
WikiGenes145216
SOURCE (Princeton)LINC00637
Genetics Home Reference (NIH)LINC00637
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00637  -     chr14:103847721-103858049 +  14q32.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00637  -     14q32.33   [Description]    (hg19-Feb_2009)
EnsemblLINC00637 - 14q32.33 [CytoView hg19]  LINC00637 - 14q32.33 [CytoView hg38]
Mapping of homologs : NCBILINC00637 [Mapview hg19]  LINC00637 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057986 BC112204 BC112206
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00637
Cluster EST : UnigeneHs.578091 [ NCBI ]
CGAP (NCI)Hs.578091
Alternative Splicing GalleryENSG00000258735
Gene ExpressionLINC00637 [ NCBI-GEO ]   LINC00637 [ EBI - ARRAY_EXPRESS ]   LINC00637 [ SEEK ]   LINC00637 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00637 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)145216
GTEX Portal (Tissue expression)LINC00637
Human Protein AtlasENSG00000258735-LINC00637 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00637
DMDM Disease mutations145216
Blocks (Seattle)LINC00637
Human Protein Atlas [tissue]ENSG00000258735-LINC00637 [tissue]
IPIIPI01025177   
Protein Interaction databases
FunCoupENSG00000258735
BioGRIDLINC00637
STRING (EMBL)LINC00637
ZODIACLINC00637
Ontologies - Pathways
Huge Navigator LINC00637 [HugePedia]
snp3D : Map Gene to Disease145216
BioCentury BCIQLINC00637
ClinGenLINC00637
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD145216
Clinical trialLINC00637
Miscellaneous
canSAR (ICR)LINC00637 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00637
EVEXLINC00637
GoPubMedLINC00637
iHOPLINC00637
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 Nov 21 13:29:44 CET 2017

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