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LINC01095 (long intergenic non-protein coding RNA 1095)

Identity

Other alias-
HGNC (Hugo) LINC01095
LocusID (NCBI) 100505545
Atlas_Id 65779
Location 4q31.22  [Link to chromosome band 4q31]
Location_base_pair Starts at 146109455 and ends at 146121913 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)LINC01095   49220
Cards
Entrez_Gene (NCBI)LINC01095  100505545  long intergenic non-protein coding RNA 1095
Aliases
GeneCards (Weizmann)LINC01095
Ensembl hg19 (Hinxton)ENSG00000248809 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000248809 [Gene_View]  chr4:146109455-146121913 [Contig_View]  LINC01095 [Vega]
ICGC DataPortalENSG00000248809
TCGA cBioPortalLINC01095
AceView (NCBI)LINC01095
Genatlas (Paris)LINC01095
WikiGenes100505545
SOURCE (Princeton)LINC01095
Genetics Home Reference (NIH)LINC01095
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01095  -     chr4:146109455-146121913 -  4q31.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01095  -     4q31.22   [Description]    (hg19-Feb_2009)
EnsemblLINC01095 - 4q31.22 [CytoView hg19]  LINC01095 - 4q31.22 [CytoView hg38]
Mapping of homologs : NCBILINC01095 [Mapview hg19]  LINC01095 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057233 BC033400 DB019632 DB525674
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01095
Cluster EST : UnigeneHs.122199 [ NCBI ]
CGAP (NCI)Hs.122199
Alternative Splicing GalleryENSG00000248809
Gene ExpressionLINC01095 [ NCBI-GEO ]   LINC01095 [ EBI - ARRAY_EXPRESS ]   LINC01095 [ SEEK ]   LINC01095 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01095 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505545
GTEX Portal (Tissue expression)LINC01095
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01095
DMDM Disease mutations100505545
Blocks (Seattle)LINC01095
Human Protein AtlasENSG00000248809
Protein Interaction databases
FunCoupENSG00000248809
BioGRIDLINC01095
STRING (EMBL)LINC01095
ZODIACLINC01095
Ontologies - Pathways
Huge Navigator LINC01095 [HugePedia]
snp3D : Map Gene to Disease100505545
BioCentury BCIQLINC01095
ClinGenLINC01095
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505545
Clinical trialLINC01095
Miscellaneous
canSAR (ICR)LINC01095 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01095
EVEXLINC01095
GoPubMedLINC01095
iHOPLINC01095
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 15:58:05 CEST 2017

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