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LINC01391 (long intergenic non-protein coding RNA 1391)

Identity

Other alias-
HGNC (Hugo) LINC01391
LocusID (NCBI) 103344930
Atlas_Id 65969
Location 3q22.3  [Link to chromosome band 3q22]
Location_base_pair Starts at 138935189 and ends at 138944020 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)LINC01391   50666
Cards
Entrez_Gene (NCBI)LINC01391  103344930  long intergenic non-protein coding RNA 1391
Aliases
GeneCards (Weizmann)LINC01391
Ensembl hg19 (Hinxton)ENSG00000244578 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000244578 [Gene_View]  chr3:138935189-138944020 [Contig_View]  LINC01391 [Vega]
ICGC DataPortalENSG00000244578
TCGA cBioPortalLINC01391
AceView (NCBI)LINC01391
Genatlas (Paris)LINC01391
WikiGenes103344930
SOURCE (Princeton)LINC01391
Genetics Home Reference (NIH)LINC01391
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01391  -     chr3:138935189-138944020 -  3q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01391  -     3q22.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01391 - 3q22.3 [CytoView hg19]  LINC01391 - 3q22.3 [CytoView hg38]
Mapping of homologs : NCBILINC01391 [Mapview hg19]  LINC01391 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK128202
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01391
Cluster EST : UnigeneHs.195033 [ NCBI ]
CGAP (NCI)Hs.195033
Alternative Splicing GalleryENSG00000244578
Gene ExpressionLINC01391 [ NCBI-GEO ]   LINC01391 [ EBI - ARRAY_EXPRESS ]   LINC01391 [ SEEK ]   LINC01391 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01391 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)103344930
GTEX Portal (Tissue expression)LINC01391
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01391
DMDM Disease mutations103344930
Blocks (Seattle)LINC01391
Human Protein AtlasENSG00000244578
Protein Interaction databases
FunCoupENSG00000244578
BioGRIDLINC01391
STRING (EMBL)LINC01391
ZODIACLINC01391
Ontologies - Pathways
Huge Navigator LINC01391 [HugePedia]
snp3D : Map Gene to Disease103344930
BioCentury BCIQLINC01391
ClinGenLINC01391
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD103344930
Clinical trialLINC01391
Miscellaneous
canSAR (ICR)LINC01391 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01391
EVEXLINC01391
GoPubMedLINC01391
iHOPLINC01391
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 : Wed Jun 7 15:58:55 CEST 2017

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