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

LINC01169 (long intergenic non-protein coding RNA 1169)

Identity

Other alias-
HGNC (Hugo) LINC01169
LocusID (NCBI) 102723165
Atlas_Id 65834
Location 15q22.31  [Link to chromosome band 15q22]
Location_base_pair Starts at 66582190 and ends at 66685798 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)LINC01169   49541
Cards
Entrez_Gene (NCBI)LINC01169  102723165  long intergenic non-protein coding RNA 1169
Aliases
GeneCards (Weizmann)LINC01169
Ensembl hg19 (Hinxton)ENSG00000259471 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000259471 [Gene_View]  chr15:66582190-66685798 [Contig_View]  LINC01169 [Vega]
ICGC DataPortalENSG00000259471
TCGA cBioPortalLINC01169
AceView (NCBI)LINC01169
Genatlas (Paris)LINC01169
WikiGenes102723165
SOURCE (Princeton)LINC01169
Genetics Home Reference (NIH)LINC01169
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01169  -     chr15:66582190-66685798 +  15q22.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01169  -     15q22.31   [Description]    (hg19-Feb_2009)
EnsemblLINC01169 - 15q22.31 [CytoView hg19]  LINC01169 - 15q22.31 [CytoView hg38]
Mapping of homologs : NCBILINC01169 [Mapview hg19]  LINC01169 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK096135 BC016970
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01169
Cluster EST : UnigeneHs.636703 [ NCBI ]
CGAP (NCI)Hs.636703
Alternative Splicing GalleryENSG00000259471
Gene ExpressionLINC01169 [ NCBI-GEO ]   LINC01169 [ EBI - ARRAY_EXPRESS ]   LINC01169 [ SEEK ]   LINC01169 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01169 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102723165
GTEX Portal (Tissue expression)LINC01169
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01169
DMDM Disease mutations102723165
Blocks (Seattle)LINC01169
Human Protein AtlasENSG00000259471
Protein Interaction databases
FunCoupENSG00000259471
BioGRIDLINC01169
STRING (EMBL)LINC01169
ZODIACLINC01169
Ontologies - Pathways
Huge Navigator LINC01169 [HugePedia]
snp3D : Map Gene to Disease102723165
BioCentury BCIQLINC01169
ClinGenLINC01169
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102723165
Clinical trialLINC01169
Miscellaneous
canSAR (ICR)LINC01169 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01169
EVEXLINC01169
GoPubMedLINC01169
iHOPLINC01169
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 : Fri May 19 11:22:01 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.