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

LINC01572 (long intergenic non-protein coding RNA 1572)

Identity

Other alias-
HGNC (Hugo) LINC01572
LocusID (NCBI) 101927957
Atlas_Id 77660
Location 16q22.2  [Link to chromosome band 16q22]
Location_base_pair Starts at 72283301 and ends at 72665009 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)LINC01572   51385
Cards
Entrez_Gene (NCBI)LINC01572  101927957  long intergenic non-protein coding RNA 1572
Aliases
GeneCards (Weizmann)LINC01572
Ensembl hg19 (Hinxton)ENSG00000261008 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261008 [Gene_View]  chr16:72283301-72665009 [Contig_View]  LINC01572 [Vega]
ICGC DataPortalENSG00000261008
TCGA cBioPortalLINC01572
AceView (NCBI)LINC01572
Genatlas (Paris)LINC01572
WikiGenes101927957
SOURCE (Princeton)LINC01572
Genetics Home Reference (NIH)LINC01572
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01572  -     chr16:72283301-72665009 -  16q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01572  -     16q22.2   [Description]    (hg19-Feb_2009)
EnsemblLINC01572 - 16q22.2 [CytoView hg19]  LINC01572 - 16q22.2 [CytoView hg38]
Mapping of homologs : NCBILINC01572 [Mapview hg19]  LINC01572 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AL525401 AL706640 BX327638 BX371395 BX483151
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01572
Cluster EST : UnigeneHs.637253 [ NCBI ]
CGAP (NCI)Hs.637253
Alternative Splicing GalleryENSG00000261008
Gene ExpressionLINC01572 [ NCBI-GEO ]   LINC01572 [ EBI - ARRAY_EXPRESS ]   LINC01572 [ SEEK ]   LINC01572 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01572 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927957
GTEX Portal (Tissue expression)LINC01572
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01572
DMDM Disease mutations101927957
Blocks (Seattle)LINC01572
Human Protein AtlasENSG00000261008
Protein Interaction databases
FunCoupENSG00000261008
BioGRIDLINC01572
STRING (EMBL)LINC01572
ZODIACLINC01572
Ontologies - Pathways
Huge Navigator LINC01572 [HugePedia]
snp3D : Map Gene to Disease101927957
BioCentury BCIQLINC01572
ClinGenLINC01572
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927957
Clinical trialLINC01572
Miscellaneous
canSAR (ICR)LINC01572 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01572
EVEXLINC01572
GoPubMedLINC01572
iHOPLINC01572
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 : Wed Jun 7 15:59:27 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.