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LINC01093 (long intergenic non-protein coding RNA 1093)

Identity

Alias (NCBI)-
HGNC (Hugo) LINC01093
LocusID (NCBI) 100506229
Atlas_Id 65777
Location 4q35.1  [Link to chromosome band 4q35]
Location_base_pair Starts at 184893000 and ends at 184899461 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)LINC01093   49218
Cards
Entrez_Gene (NCBI)LINC01093  100506229  long intergenic non-protein coding RNA 1093
Aliases
GeneCards (Weizmann)LINC01093
Ensembl hg19 (Hinxton)ENSG00000249173 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000249173 [Gene_View]  ENSG00000249173 [Sequence]  chr4:184893000-184899461 [Contig_View]  LINC01093 [Vega]
ICGC DataPortalENSG00000249173
TCGA cBioPortalLINC01093
AceView (NCBI)LINC01093
Genatlas (Paris)LINC01093
WikiGenes100506229
SOURCE (Princeton)LINC01093
Genetics Home Reference (NIH)LINC01093
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01093  -     chr4:184893000-184899461 -  4q35.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01093  -     4q35.1   [Description]    (hg19-Feb_2009)
GoldenPathLINC01093 - 4q35.1 [CytoView hg19]  LINC01093 - 4q35.1 [CytoView hg38]
ImmunoBaseENSG00000249173
genome Data Viewer NCBILINC01093 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AK096134 AY429594 AY429595 CB153796
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01093
Alternative Splicing GalleryENSG00000249173
Gene ExpressionLINC01093 [ NCBI-GEO ]   LINC01093 [ EBI - ARRAY_EXPRESS ]   LINC01093 [ SEEK ]   LINC01093 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01093 [ Firebrowse - Broad ]
GenevisibleExpression of LINC01093 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100506229
GTEX Portal (Tissue expression)LINC01093
Human Protein AtlasENSG00000249173-LINC01093 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01093
DMDM Disease mutations100506229
Blocks (Seattle)LINC01093
Human Protein Atlas [tissue]ENSG00000249173-LINC01093 [tissue]
Protein Interaction databases
FunCoupENSG00000249173
BioGRIDLINC01093
STRING (EMBL)LINC01093
ZODIACLINC01093
Ontologies - Pathways
Huge Navigator LINC01093 [HugePedia]
snp3D : Map Gene to Disease100506229
BioCentury BCIQLINC01093
ClinGenLINC01093
Clinical trials, drugs, therapy
Protein Interactions : CTD100506229
Clinical trialLINC01093
Miscellaneous
canSAR (ICR)LINC01093 (select the gene name)
HarmonizomeLINC01093
DataMed IndexLINC01093
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01093
EVEXLINC01093
GoPubMedLINC01093
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 : Sat Aug 22 19:16:44 CEST 2020

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