Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

LINC01602 (long intergenic non-protein coding RNA 1602)

Identity

Alias_symbol (synonym)T1560
Other alias
HGNC (Hugo) LINC01602
LocusID (NCBI) 100505477
Atlas_Id 74447
Location 8q12.1  [Link to chromosome band 8q12]
Location_base_pair Starts at 57978358 and ends at 57984126 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)LINC01602   51634
Cards
Entrez_Gene (NCBI)LINC01602  100505477  long intergenic non-protein coding RNA 1602
AliasesT1560
GeneCards (Weizmann)LINC01602
Ensembl hg19 (Hinxton)ENSG00000205293 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000205293 [Gene_View]  chr8:57978358-57984126 [Contig_View]  LINC01602 [Vega]
ICGC DataPortalENSG00000205293
TCGA cBioPortalLINC01602
AceView (NCBI)LINC01602
Genatlas (Paris)LINC01602
WikiGenes100505477
SOURCE (Princeton)LINC01602
Genetics Home Reference (NIH)LINC01602
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01602  -     chr8:57978358-57984126 +  8q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01602  -     8q12.1   [Description]    (hg19-Feb_2009)
EnsemblLINC01602 - 8q12.1 [CytoView hg19]  LINC01602 - 8q12.1 [CytoView hg38]
Mapping of homologs : NCBILINC01602 [Mapview hg19]  LINC01602 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB111913 BC040611 BC130491 BC130493
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01602
Cluster EST : UnigeneHs.434693 [ NCBI ]
CGAP (NCI)Hs.434693
Alternative Splicing GalleryENSG00000205293
Gene ExpressionLINC01602 [ NCBI-GEO ]   LINC01602 [ EBI - ARRAY_EXPRESS ]   LINC01602 [ SEEK ]   LINC01602 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01602 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505477
GTEX Portal (Tissue expression)LINC01602
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01602
DMDM Disease mutations100505477
Blocks (Seattle)LINC01602
Human Protein AtlasENSG00000205293
IPIIPI00444543   
Protein Interaction databases
FunCoupENSG00000205293
BioGRIDLINC01602
STRING (EMBL)LINC01602
ZODIACLINC01602
Ontologies - Pathways
Huge Navigator LINC01602 [HugePedia]
snp3D : Map Gene to Disease100505477
BioCentury BCIQLINC01602
ClinGenLINC01602
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505477
Clinical trialLINC01602
Miscellaneous
canSAR (ICR)LINC01602 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01602
EVEXLINC01602
GoPubMedLINC01602
iHOPLINC01602
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 : Mon Sep 18 13:14:55 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.