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LINC01029 (long intergenic non-protein coding RNA 1029)

Identity

Alias (NCBI)-
HGNC (Hugo) LINC01029
LocusID (NCBI) 101927715
Atlas_Id 65746
Location 18q23  [Link to chromosome band 18q23]
Location_base_pair Starts at 77971296 and ends at 77993727 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)LINC01029   49015
Cards
Entrez_Gene (NCBI)LINC01029  101927715  long intergenic non-protein coding RNA 1029
Aliases
GeneCards (Weizmann)LINC01029
Ensembl hg19 (Hinxton)ENSG00000265843 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265843 [Gene_View]  ENSG00000265843 [Sequence]  chr18:77971296-77993727 [Contig_View]  LINC01029 [Vega]
ICGC DataPortalENSG00000265843
TCGA cBioPortalLINC01029
AceView (NCBI)LINC01029
Genatlas (Paris)LINC01029
WikiGenes101927715
SOURCE (Princeton)LINC01029
Genetics Home Reference (NIH)LINC01029
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01029  -     chr18:77971296-77993727 -  18q23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01029  -     18q23   [Description]    (hg19-Feb_2009)
GoldenPathLINC01029 - 18q23 [CytoView hg19]  LINC01029 - 18q23 [CytoView hg38]
ImmunoBaseENSG00000265843
genome Data Viewer NCBILINC01029 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)BC016792 BF183892
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01029
Alternative Splicing GalleryENSG00000265843
Gene ExpressionLINC01029 [ NCBI-GEO ]   LINC01029 [ EBI - ARRAY_EXPRESS ]   LINC01029 [ SEEK ]   LINC01029 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01029 [ Firebrowse - Broad ]
GenevisibleExpression of LINC01029 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101927715
GTEX Portal (Tissue expression)LINC01029
Human Protein AtlasENSG00000265843-LINC01029 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01029
DMDM Disease mutations101927715
Blocks (Seattle)LINC01029
Human Protein Atlas [tissue]ENSG00000265843-LINC01029 [tissue]
Protein Interaction databases
FunCoupENSG00000265843
BioGRIDLINC01029
STRING (EMBL)LINC01029
ZODIACLINC01029
Ontologies - Pathways
Huge Navigator LINC01029 [HugePedia]
snp3D : Map Gene to Disease101927715
BioCentury BCIQLINC01029
ClinGenLINC01029
Clinical trials, drugs, therapy
Protein Interactions : CTD101927715
Clinical trialLINC01029
Miscellaneous
canSAR (ICR)LINC01029 (select the gene name)
HarmonizomeLINC01029
DataMed IndexLINC01029
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01029
EVEXLINC01029
GoPubMedLINC01029
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 : Thu Jul 16 16:02:27 CEST 2020

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