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LINC01057 (long intergenic non-protein coding RNA 1057)

Identity

Other alias-
HGNC (Hugo) LINC01057
LocusID (NCBI) 101928079
Atlas_Id 65760
Location 1p21.3  [Link to chromosome band 1p21]
Location_base_pair Starts at 95123089 and ends at 95285837 bp from pter ( according to hg19-Feb_2009)

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)LINC01057   49057
Cards
Entrez_Gene (NCBI)LINC01057  101928079  long intergenic non-protein coding RNA 1057
Aliases
GeneCards (Weizmann)LINC01057
Ensembl hg19 (Hinxton)ENSG00000224081 [Gene_View]  chr1:95123089-95285837 [Contig_View]  LINC01057 [Vega]
Ensembl hg38 (Hinxton)ENSG00000224081 [Gene_View]  chr1:95123089-95285837 [Contig_View]  LINC01057 [Vega]
ICGC DataPortalENSG00000224081
TCGA cBioPortalLINC01057
AceView (NCBI)LINC01057
Genatlas (Paris)LINC01057
WikiGenes101928079
SOURCE (Princeton)LINC01057
Genetics Home Reference (NIH)LINC01057
Genomic and cartography
GoldenPath hg19 (UCSC)LINC01057  -     chr1:95123089-95285837 -  1p21.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LINC01057  -     1p21.3   [Description]    (hg38-Dec_2013)
EnsemblLINC01057 - 1p21.3 [CytoView hg19]  LINC01057 - 1p21.3 [CytoView hg38]
Mapping of homologs : NCBILINC01057 [Mapview hg19]  LINC01057 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC030750 HG492275 HG492276 HG492277 HG492278
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929290
Consensus coding sequences : CCDS (NCBI)LINC01057
Cluster EST : UnigeneHs.596857 [ NCBI ]
CGAP (NCI)Hs.596857
Alternative Splicing GalleryENSG00000224081
Gene ExpressionLINC01057 [ NCBI-GEO ]   LINC01057 [ EBI - ARRAY_EXPRESS ]   LINC01057 [ SEEK ]   LINC01057 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01057 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928079
GTEX Portal (Tissue expression)LINC01057
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01057
DMDM Disease mutations101928079
Blocks (Seattle)LINC01057
Human Protein AtlasENSG00000224081
Protein Interaction databases
FunCoupENSG00000224081
BioGRIDLINC01057
STRING (EMBL)LINC01057
ZODIACLINC01057
Ontologies - Pathways
Huge Navigator LINC01057 [HugePedia]
snp3D : Map Gene to Disease101928079
BioCentury BCIQLINC01057
ClinGenLINC01057
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928079
Clinical trialLINC01057
Miscellaneous
canSAR (ICR)LINC01057 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01057
EVEXLINC01057
GoPubMedLINC01057
iHOPLINC01057
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 : Tue Mar 14 12:12:58 CET 2017

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