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LINC01692 (long intergenic non-protein coding RNA 1692)

Identity

Other alias-
HGNC (Hugo) LINC01692
LocusID (NCBI) 339622
Atlas_Id 78951
Location 21q21.2  [Link to chromosome band 21q21]
Location_base_pair Starts at 24840550 and ends at 25057743 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)LINC01692   52480
Cards
Entrez_Gene (NCBI)LINC01692  339622  long intergenic non-protein coding RNA 1692
Aliases
GeneCards (Weizmann)LINC01692
Ensembl hg19 (Hinxton)ENSG00000226983 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226983 [Gene_View]  chr21:24840550-25057743 [Contig_View]  LINC01692 [Vega]
ICGC DataPortalENSG00000226983
TCGA cBioPortalLINC01692
AceView (NCBI)LINC01692
Genatlas (Paris)LINC01692
WikiGenes339622
SOURCE (Princeton)LINC01692
Genetics Home Reference (NIH)LINC01692
Genomic and cartography
GoldenPath hg38 (UCSC)LINC01692  -     chr21:24840550-25057743 +  21q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LINC01692  -     21q21.2   [Description]    (hg19-Feb_2009)
EnsemblLINC01692 - 21q21.2 [CytoView hg19]  LINC01692 - 21q21.2 [CytoView hg38]
Mapping of homologs : NCBILINC01692 [Mapview hg19]  LINC01692 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC040319
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LINC01692
Cluster EST : UnigeneHs.616316 [ NCBI ]
CGAP (NCI)Hs.616316
Alternative Splicing GalleryENSG00000226983
Gene ExpressionLINC01692 [ NCBI-GEO ]   LINC01692 [ EBI - ARRAY_EXPRESS ]   LINC01692 [ SEEK ]   LINC01692 [ MEM ]
Gene Expression Viewer (FireBrowse)LINC01692 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)339622
GTEX Portal (Tissue expression)LINC01692
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LINC01692
DMDM Disease mutations339622
Blocks (Seattle)LINC01692
Human Protein AtlasENSG00000226983
Protein Interaction databases
FunCoupENSG00000226983
BioGRIDLINC01692
STRING (EMBL)LINC01692
ZODIACLINC01692
Ontologies - Pathways
Huge Navigator LINC01692 [HugePedia]
snp3D : Map Gene to Disease339622
BioCentury BCIQLINC01692
ClinGenLINC01692
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD339622
Clinical trialLINC01692
Miscellaneous
canSAR (ICR)LINC01692 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLINC01692
EVEXLINC01692
GoPubMedLINC01692
iHOPLINC01692
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 13:15:06 CEST 2017

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