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LINC02446 (long intergenic non-protein coding RNA 2446)

Identity

Other alias-
HGNC (Hugo) LINC02446
LocusID (NCBI) 101060038
Atlas_Id 79167
Location 12p13.2  [Link to chromosome band 12p13]
Location_base_pair Starts at 10553379 and ends at 10558794 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)LINC02446   53378
Cards
Entrez_Gene (NCBI)LINC02446  101060038  long intergenic non-protein coding RNA 2446
Aliases
GeneCards (Weizmann)LINC02446
Ensembl hg19 (Hinxton)ENSG00000256039 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000256039 [Gene_View]  chr12:10553379-10558794 [Contig_View]  LINC02446 [Vega]
ICGC DataPortalENSG00000256039
TCGA cBioPortalLINC02446
AceView (NCBI)LINC02446
Genatlas (Paris)LINC02446
WikiGenes101060038
SOURCE (Princeton)LINC02446
Genetics Home Reference (NIH)LINC02446
Genomic and cartography
GoldenPath hg38 (UCSC)LINC02446  -     chr12:10553379-10558794 +  12p13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC02446  -     12p13.2   [Description]    (hg19-Feb_2009)
EnsemblLINC02446 - 12p13.2 [CytoView hg19]  LINC02446 - 12p13.2 [CytoView hg38]
Mapping of homologs : NCBILINC02446 [Mapview hg19]  LINC02446 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC02446
Alternative Splicing GalleryENSG00000256039
Gene ExpressionLINC02446 [ NCBI-GEO ]   LINC02446 [ EBI - ARRAY_EXPRESS ]   LINC02446 [ SEEK ]   LINC02446 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC02446 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101060038
GTEX Portal (Tissue expression)LINC02446
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC02446
DMDM Disease mutations101060038
Blocks (Seattle)LINC02446
Human Protein AtlasENSG00000256039
Protein Interaction databases
FunCoupENSG00000256039
BioGRIDLINC02446
STRING (EMBL)LINC02446
ZODIACLINC02446
Ontologies - Pathways
Huge Navigator LINC02446 [HugePedia]
snp3D : Map Gene to Disease101060038
BioCentury BCIQLINC02446
ClinGenLINC02446
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101060038
Clinical trialLINC02446
Miscellaneous
canSAR (ICR)LINC02446 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC02446
EVEXLINC02446
GoPubMedLINC02446
iHOPLINC02446
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Sep 18 13:16:29 CEST 2017

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