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LINC01022 (long intergenic non-protein coding RNA 1022)

Identity

Alias_symbol (synonym)TCONS_00013107
Other alias-
HGNC (Hugo) LINC01022
LocusID (NCBI) 105375616
Atlas_Id 77795
Location 7q36.3  [Link to chromosome band 7q36]
Location_base_pair Starts at 158590629 and ends at 158591933 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LINC01022   48998
Cards
Entrez_Gene (NCBI)LINC01022  105375616  long intergenic non-protein coding RNA 1022
Aliases
GeneCards (Weizmann)LINC01022
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr7:158590629-158591933 [Contig_View]  LINC01022 [Vega]
TCGA cBioPortalLINC01022
AceView (NCBI)LINC01022
Genatlas (Paris)LINC01022
WikiGenes105375616
SOURCE (Princeton)LINC01022
Genetics Home Reference (NIH)LINC01022
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01022  -     chr7:158590629-158591933 +  7q36.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01022  -     7q36.3   [Description]    (hg19-Feb_2009)
EnsemblLINC01022 - 7q36.3 [CytoView hg19]  LINC01022 - 7q36.3 [CytoView hg38]
Mapping of homologs : NCBILINC01022 [Mapview hg19]  LINC01022 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA993709 DB337926 DB518621
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01022
Cluster EST : UnigeneHs.641681 [ NCBI ]
CGAP (NCI)Hs.641681
Gene ExpressionLINC01022 [ NCBI-GEO ]   LINC01022 [ EBI - ARRAY_EXPRESS ]   LINC01022 [ SEEK ]   LINC01022 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01022 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105375616
GTEX Portal (Tissue expression)LINC01022
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01022
DMDM Disease mutations105375616
Blocks (Seattle)LINC01022
Protein Interaction databases
BioGRIDLINC01022
STRING (EMBL)LINC01022
ZODIACLINC01022
Ontologies - Pathways
Huge Navigator LINC01022 [HugePedia]
snp3D : Map Gene to Disease105375616
BioCentury BCIQLINC01022
ClinGenLINC01022
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105375616
Clinical trialLINC01022
Miscellaneous
canSAR (ICR)LINC01022 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01022
EVEXLINC01022
GoPubMedLINC01022
iHOPLINC01022
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 : Thu Nov 9 11:55:21 CET 2017

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