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LINC00351 (long intergenic non-protein coding RNA 351)

Identity

Other alias-
HGNC (Hugo) LINC00351
LocusID (NCBI) 100874137
Atlas_Id 65387
Location 13q31.1  [Link to chromosome band 13q31]
Location_base_pair Starts at 85363603 and ends at 85544662 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)LINC00351   42669
Cards
Entrez_Gene (NCBI)LINC00351  100874137  long intergenic non-protein coding RNA 351
Aliases
GeneCards (Weizmann)LINC00351
Ensembl hg19 (Hinxton)ENSG00000226317 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226317 [Gene_View]  chr13:85363603-85544662 [Contig_View]  LINC00351 [Vega]
ICGC DataPortalENSG00000226317
TCGA cBioPortalLINC00351
AceView (NCBI)LINC00351
Genatlas (Paris)LINC00351
WikiGenes100874137
SOURCE (Princeton)LINC00351
Genetics Home Reference (NIH)LINC00351
Genomic and cartography
GoldenPath hg38 (UCSC)LINC00351  -     chr13:85363603-85544662 +  13q31.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC00351  -     13q31.1   [Description]    (hg19-Feb_2009)
EnsemblLINC00351 - 13q31.1 [CytoView hg19]  LINC00351 - 13q31.1 [CytoView hg38]
Mapping of homologs : NCBILINC00351 [Mapview hg19]  LINC00351 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BM559680
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC00351
Cluster EST : UnigeneHs.742643 [ NCBI ]
CGAP (NCI)Hs.742643
Alternative Splicing GalleryENSG00000226317
Gene ExpressionLINC00351 [ NCBI-GEO ]   LINC00351 [ EBI - ARRAY_EXPRESS ]   LINC00351 [ SEEK ]   LINC00351 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC00351 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100874137
GTEX Portal (Tissue expression)LINC00351
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC00351
DMDM Disease mutations100874137
Blocks (Seattle)LINC00351
Human Protein AtlasENSG00000226317
Protein Interaction databases
FunCoupENSG00000226317
BioGRIDLINC00351
STRING (EMBL)LINC00351
ZODIACLINC00351
Ontologies - Pathways
Huge Navigator LINC00351 [HugePedia]
snp3D : Map Gene to Disease100874137
BioCentury BCIQLINC00351
ClinGenLINC00351
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100874137
Clinical trialLINC00351
Miscellaneous
canSAR (ICR)LINC00351 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC00351
EVEXLINC00351
GoPubMedLINC00351
iHOPLINC00351
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 13:13:00 CEST 2017

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