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LINC01102 (long intergenic non-protein coding RNA 1102)

Identity

Other alias-
HGNC (Hugo) LINC01102
LocusID (NCBI) 150568
Atlas_Id 65786
Location 2q12.1  [Link to chromosome band 2q12]
Location_base_pair Starts at 104434347 and ends at 104512757 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)LINC01102   27165
Cards
Entrez_Gene (NCBI)LINC01102  150568  long intergenic non-protein coding RNA 1102
Aliases
GeneCards (Weizmann)LINC01102
Ensembl hg19 (Hinxton)ENSG00000235597 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000235597 [Gene_View]  chr2:104434347-104512757 [Contig_View]  LINC01102 [Vega]
ICGC DataPortalENSG00000235597
TCGA cBioPortalLINC01102
AceView (NCBI)LINC01102
Genatlas (Paris)LINC01102
WikiGenes150568
SOURCE (Princeton)LINC01102
Genetics Home Reference (NIH)LINC01102
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01102  -     chr2:104434347-104512757 +  2q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01102  -     2q12.1   [Description]    (hg19-Feb_2009)
EnsemblLINC01102 - 2q12.1 [CytoView hg19]  LINC01102 - 2q12.1 [CytoView hg38]
Mapping of homologs : NCBILINC01102 [Mapview hg19]  LINC01102 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK055090 AK126958 AL137513 BC105699 BC105700
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01102
Cluster EST : UnigeneHs.107284 [ NCBI ]
CGAP (NCI)Hs.107284
Alternative Splicing GalleryENSG00000235597
Gene ExpressionLINC01102 [ NCBI-GEO ]   LINC01102 [ EBI - ARRAY_EXPRESS ]   LINC01102 [ SEEK ]   LINC01102 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01102 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)150568
GTEX Portal (Tissue expression)LINC01102
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01102
DMDM Disease mutations150568
Blocks (Seattle)LINC01102
Human Protein AtlasENSG00000235597
Protein Interaction databases
FunCoupENSG00000235597
BioGRIDLINC01102
STRING (EMBL)LINC01102
ZODIACLINC01102
Ontologies - Pathways
Huge Navigator LINC01102 [HugePedia]
snp3D : Map Gene to Disease150568
BioCentury BCIQLINC01102
ClinGenLINC01102
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD150568
Clinical trialLINC01102
Miscellaneous
canSAR (ICR)LINC01102 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01102
EVEXLINC01102
GoPubMedLINC01102
iHOPLINC01102
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 15:58:07 CEST 2017

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