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LINC00632 (long intergenic non-protein coding RNA 632)

Identity

Other alias-
HGNC (Hugo) LINC00632
LocusID (NCBI) 286411
Atlas_Id 65547
Location Xq27.1  [Link to chromosome band Xq27]
Location_base_pair Starts at 139791924 and ends at 139796996 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)LINC00632   27865
Cards
Entrez_Gene (NCBI)LINC00632  286411  long intergenic non-protein coding RNA 632
Aliases
GeneCards (Weizmann)LINC00632
Ensembl hg19 (Hinxton)ENSG00000203930 [Gene_View]  chrX:139791924-139796996 [Contig_View]  LINC00632 [Vega]
Ensembl hg38 (Hinxton)ENSG00000203930 [Gene_View]  chrX:139791924-139796996 [Contig_View]  LINC00632 [Vega]
ICGC DataPortalENSG00000203930
TCGA cBioPortalLINC00632
AceView (NCBI)LINC00632
Genatlas (Paris)LINC00632
WikiGenes286411
SOURCE (Princeton)LINC00632
Genetics Home Reference (NIH)LINC00632
Genomic and cartography
GoldenPath hg19 (UCSC)LINC00632  -     chrX:139791924-139796996 +  Xq27.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LINC00632  -     Xq27.1   [Description]    (hg38-Dec_2013)
EnsemblLINC00632 - Xq27.1 [CytoView hg19]  LINC00632 - Xq27.1 [CytoView hg38]
Mapping of homologs : NCBILINC00632 [Mapview hg19]  LINC00632 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK054978 BM811380 BQ343502 BX508035 DA082671
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000023 NC_018934 NT_011786 NW_004929446
Consensus coding sequences : CCDS (NCBI)LINC00632
Cluster EST : UnigeneHs.317627 [ NCBI ]
CGAP (NCI)Hs.317627
Alternative Splicing GalleryENSG00000203930
Gene ExpressionLINC00632 [ NCBI-GEO ]   LINC00632 [ EBI - ARRAY_EXPRESS ]   LINC00632 [ SEEK ]   LINC00632 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00632 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)286411
GTEX Portal (Tissue expression)LINC00632
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00632
DMDM Disease mutations286411
Blocks (Seattle)LINC00632
Human Protein AtlasENSG00000203930
IPIIPI00552977   
Protein Interaction databases
FunCoupENSG00000203930
BioGRIDLINC00632
STRING (EMBL)LINC00632
ZODIACLINC00632
Ontologies - Pathways
Huge Navigator LINC00632 [HugePedia]
snp3D : Map Gene to Disease286411
BioCentury BCIQLINC00632
ClinGenLINC00632
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD286411
Clinical trialLINC00632
Miscellaneous
canSAR (ICR)LINC00632 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00632
EVEXLINC00632
GoPubMedLINC00632
iHOPLINC00632
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 : Tue Mar 14 12:12:09 CET 2017

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