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

LINC01669 (long intergenic non-protein coding RNA 1669)

Identity

Other alias-
HGNC (Hugo) LINC01669
LocusID (NCBI) 102724354
Atlas_Id 79946
Location 21q22.3  [Link to chromosome band 21q22]
Location_base_pair Starts at 43461960 and ends at 43479534 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)LINC01669   52457
Cards
Entrez_Gene (NCBI)LINC01669  102724354  long intergenic non-protein coding RNA 1669
Aliases
GeneCards (Weizmann)LINC01669
Ensembl hg19 (Hinxton)ENSG00000280191 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000280191 [Gene_View]  chr21:43461960-43479534 [Contig_View]  LINC01669 [Vega]
ICGC DataPortalENSG00000280191
TCGA cBioPortalLINC01669
AceView (NCBI)LINC01669
Genatlas (Paris)LINC01669
WikiGenes102724354
SOURCE (Princeton)LINC01669
Genetics Home Reference (NIH)LINC01669
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01669  -     chr21:43461960-43479534 -  21q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01669  -     21q22.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01669 - 21q22.3 [CytoView hg19]  LINC01669 - 21q22.3 [CytoView hg38]
Mapping of homologs : NCBILINC01669 [Mapview hg19]  LINC01669 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA868532 AW206028 HY162931 HY359299
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01669
Cluster EST : UnigeneHs.592161 [ NCBI ]
CGAP (NCI)Hs.592161
Alternative Splicing GalleryENSG00000280191
Gene ExpressionLINC01669 [ NCBI-GEO ]   LINC01669 [ EBI - ARRAY_EXPRESS ]   LINC01669 [ SEEK ]   LINC01669 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01669 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102724354
GTEX Portal (Tissue expression)LINC01669
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01669
DMDM Disease mutations102724354
Blocks (Seattle)LINC01669
Human Protein AtlasENSG00000280191
Protein Interaction databases
FunCoupENSG00000280191
BioGRIDLINC01669
STRING (EMBL)LINC01669
ZODIACLINC01669
Ontologies - Pathways
Huge Navigator LINC01669 [HugePedia]
snp3D : Map Gene to Disease102724354
BioCentury BCIQLINC01669
ClinGenLINC01669
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102724354
Clinical trialLINC01669
Miscellaneous
canSAR (ICR)LINC01669 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01669
EVEXLINC01669
GoPubMedLINC01669
iHOPLINC01669
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 13:15:03 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.