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LINC01775 (long intergenic non-protein coding RNA 1775)

Identity

Other alias-
HGNC (Hugo) LINC01775
LocusID (NCBI) 101928602
Atlas_Id 79068
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 2458937 and ends at 2462185 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)LINC01775   52565
Cards
Entrez_Gene (NCBI)LINC01775  101928602  long intergenic non-protein coding RNA 1775
Aliases
GeneCards (Weizmann)LINC01775
Ensembl hg19 (Hinxton)ENSG00000267201 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267201 [Gene_View]  chr19:2458937-2462185 [Contig_View]  LINC01775 [Vega]
ICGC DataPortalENSG00000267201
TCGA cBioPortalLINC01775
AceView (NCBI)LINC01775
Genatlas (Paris)LINC01775
WikiGenes101928602
SOURCE (Princeton)LINC01775
Genetics Home Reference (NIH)LINC01775
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01775  -     chr19:2458937-2462185 -  19p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01775  -     19p13.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01775 - 19p13.3 [CytoView hg19]  LINC01775 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBILINC01775 [Mapview hg19]  LINC01775 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC040839
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01775
Cluster EST : UnigeneHs.541407 [ NCBI ]
CGAP (NCI)Hs.541407
Alternative Splicing GalleryENSG00000267201
Gene ExpressionLINC01775 [ NCBI-GEO ]   LINC01775 [ EBI - ARRAY_EXPRESS ]   LINC01775 [ SEEK ]   LINC01775 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01775 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928602
GTEX Portal (Tissue expression)LINC01775
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01775
DMDM Disease mutations101928602
Blocks (Seattle)LINC01775
Human Protein AtlasENSG00000267201
Protein Interaction databases
FunCoupENSG00000267201
BioGRIDLINC01775
STRING (EMBL)LINC01775
ZODIACLINC01775
Ontologies - Pathways
Huge Navigator LINC01775 [HugePedia]
snp3D : Map Gene to Disease101928602
BioCentury BCIQLINC01775
ClinGenLINC01775
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928602
Clinical trialLINC01775
Miscellaneous
canSAR (ICR)LINC01775 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01775
EVEXLINC01775
GoPubMedLINC01775
iHOPLINC01775
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 13:15:17 CEST 2017

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