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RNVU1-1 (RNA, variant U1 small nuclear 1)

Identity

Alias_namesRNU1P10
RNU1-10P
RNVU1-10
RNA, U1 small nuclear pseudogene 10
RNA, U1 small nuclear 10, pseudogene
RNA, variant U1 small nuclear 10
Alias_symbol (synonym)vU1.1
U1P14
U1.4
vU1.10
RNU1-53
Other alias
HGNC (Hugo) RNVU1-1
LocusID (NCBI) 101954273
Atlas_Id 79260
Location 1q21.2  [Link to chromosome band 1q21]
Location_base_pair Starts at 148362370 and ends at 148362533 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)RNVU1-1   10133
Cards
Entrez_Gene (NCBI)RNVU1-1  101954273  RNA, variant U1 small nuclear 1
AliasesRNU1-10P; RNU1-53; RNU1P10; RNVU1-10; 
U1.4; U1P14; vU1.1; vU1.10
GeneCards (Weizmann)RNVU1-1
Ensembl hg19 (Hinxton)ENSG00000207340 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207340 [Gene_View]  chr1:148362370-148362533 [Contig_View]  RNVU1-1 [Vega]
ICGC DataPortalENSG00000207340
TCGA cBioPortalRNVU1-1
AceView (NCBI)RNVU1-1
Genatlas (Paris)RNVU1-1
WikiGenes101954273
SOURCE (Princeton)RNVU1-1
Genetics Home Reference (NIH)RNVU1-1
Genomic and cartography
GoldenPath hg38 (UCSC)RNVU1-1  -     chr1:148362370-148362533 -  1q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RNVU1-1  -     1q21.2   [Description]    (hg19-Feb_2009)
EnsemblRNVU1-1 - 1q21.2 [CytoView hg19]  RNVU1-1 - 1q21.2 [CytoView hg38]
Mapping of homologs : NCBIRNVU1-1 [Mapview hg19]  RNVU1-1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RNVU1-1
Alternative Splicing GalleryENSG00000207340
Gene ExpressionRNVU1-1 [ NCBI-GEO ]   RNVU1-1 [ EBI - ARRAY_EXPRESS ]   RNVU1-1 [ SEEK ]   RNVU1-1 [ MEM ]
Gene Expression Viewer (FireBrowse)RNVU1-1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101954273
GTEX Portal (Tissue expression)RNVU1-1
Human Protein AtlasENSG00000207340-RNVU1-1 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)RNVU1-1
DMDM Disease mutations101954273
Blocks (Seattle)RNVU1-1
Human Protein Atlas [tissue]ENSG00000207340-RNVU1-1 [tissue]
Protein Interaction databases
FunCoupENSG00000207340
BioGRIDRNVU1-1
STRING (EMBL)RNVU1-1
ZODIACRNVU1-1
Ontologies - Pathways
Huge Navigator RNVU1-1 [HugePedia]
snp3D : Map Gene to Disease101954273
BioCentury BCIQRNVU1-1
ClinGenRNVU1-1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101954273
Clinical trialRNVU1-1
Miscellaneous
canSAR (ICR)RNVU1-1 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRNVU1-1
EVEXRNVU1-1
GoPubMedRNVU1-1
iHOPRNVU1-1
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 : Tue Nov 21 13:02:40 CET 2017

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