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LINC01098 (long intergenic non-protein coding RNA 1098)

Identity

Other alias-
HGNC (Hugo) LINC01098
LocusID (NCBI) 285501
Atlas_Id 65782
Location 4q34.3  [Link to chromosome band 4q34]
Location_base_pair Starts at 177728757 and ends at 177990750 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)LINC01098   27731
Cards
Entrez_Gene (NCBI)LINC01098  285501  long intergenic non-protein coding RNA 1098
Aliases
GeneCards (Weizmann)LINC01098
Ensembl hg19 (Hinxton)ENSG00000231171 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000231171 [Gene_View]  chr4:177728757-177990750 [Contig_View]  LINC01098 [Vega]
ICGC DataPortalENSG00000231171
TCGA cBioPortalLINC01098
AceView (NCBI)LINC01098
Genatlas (Paris)LINC01098
WikiGenes285501
SOURCE (Princeton)LINC01098
Genetics Home Reference (NIH)LINC01098
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01098  -     chr4:177728757-177990750 +  4q34.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01098  -     4q34.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01098 - 4q34.3 [CytoView hg19]  LINC01098 - 4q34.3 [CytoView hg38]
Mapping of homologs : NCBILINC01098 [Mapview hg19]  LINC01098 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033326 BC113482 BC113484
RefSeq transcript (Entrez)NM_001085490
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01098
Cluster EST : UnigeneHs.722466 [ NCBI ]
CGAP (NCI)Hs.722466
Alternative Splicing GalleryENSG00000231171
Gene ExpressionLINC01098 [ NCBI-GEO ]   LINC01098 [ EBI - ARRAY_EXPRESS ]   LINC01098 [ SEEK ]   LINC01098 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01098 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)285501
GTEX Portal (Tissue expression)LINC01098
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01098
DMDM Disease mutations285501
Blocks (Seattle)LINC01098
Human Protein AtlasENSG00000231171
IPIIPI00848252   
Protein Interaction databases
FunCoupENSG00000231171
BioGRIDLINC01098
STRING (EMBL)LINC01098
ZODIACLINC01098
Ontologies - Pathways
Huge Navigator LINC01098 [HugePedia]
snp3D : Map Gene to Disease285501
BioCentury BCIQLINC01098
ClinGenLINC01098
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD285501
Clinical trialLINC01098
Miscellaneous
canSAR (ICR)LINC01098 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01098
EVEXLINC01098
GoPubMedLINC01098
iHOPLINC01098
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 15:58:06 CEST 2017

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