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LINC01749 (long intergenic non-protein coding RNA 1749)

Identity

Other alias-
HGNC (Hugo) LINC01749
LocusID (NCBI) 63930
Atlas_Id 80011
Location 20q13.33  [Link to chromosome band 20q13]
Location_base_pair Starts at 63009383 and ends at 63085071 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)LINC01749   52537
Cards
Entrez_Gene (NCBI)LINC01749  63930  long intergenic non-protein coding RNA 1749
Aliases
GeneCards (Weizmann)LINC01749
Ensembl hg19 (Hinxton)ENSG00000272259 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000272259 [Gene_View]  chr20:63009383-63085071 [Contig_View]  LINC01749 [Vega]
ICGC DataPortalENSG00000272259
TCGA cBioPortalLINC01749
AceView (NCBI)LINC01749
Genatlas (Paris)LINC01749
WikiGenes63930
SOURCE (Princeton)LINC01749
Genetics Home Reference (NIH)LINC01749
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01749  -     chr20:63009383-63085071 +  20q13.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01749  -     20q13.33   [Description]    (hg19-Feb_2009)
EnsemblLINC01749 - 20q13.33 [CytoView hg19]  LINC01749 - 20q13.33 [CytoView hg38]
Mapping of homologs : NCBILINC01749 [Mapview hg19]  LINC01749 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK128329 AK310606
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01749
Cluster EST : UnigeneHs.640084 [ NCBI ]
CGAP (NCI)Hs.640084
Alternative Splicing GalleryENSG00000272259
Gene ExpressionLINC01749 [ NCBI-GEO ]   LINC01749 [ EBI - ARRAY_EXPRESS ]   LINC01749 [ SEEK ]   LINC01749 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01749 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)63930
GTEX Portal (Tissue expression)LINC01749
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01749
DMDM Disease mutations63930
Blocks (Seattle)LINC01749
Human Protein AtlasENSG00000272259
IPIIPI00443800   
Protein Interaction databases
FunCoupENSG00000272259
BioGRIDLINC01749
STRING (EMBL)LINC01749
ZODIACLINC01749
Ontologies - Pathways
Huge Navigator LINC01749 [HugePedia]
snp3D : Map Gene to Disease63930
BioCentury BCIQLINC01749
ClinGenLINC01749
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD63930
Clinical trialLINC01749
Miscellaneous
canSAR (ICR)LINC01749 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01749
EVEXLINC01749
GoPubMedLINC01749
iHOPLINC01749
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 : Mon Sep 18 13:15:14 CEST 2017

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