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RNVU1-19 (RNA, variant U1 small nuclear 19)

Identity

Alias_namesRNVU1-13
RNA, variant U1 small nuclear 13
Alias_symbol (synonym)vU1.19
RNU1-126
vU1.13
RNU1-147
Other alias
HGNC (Hugo) RNVU1-19
LocusID (NCBI) 101954277
Atlas_Id 72757
Location 1p11.2  [Link to chromosome band 1p11]
Location_base_pair Starts at 120850819 and ends at 120850985 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)RNVU1-19   48324
Cards
Entrez_Gene (NCBI)RNVU1-19  101954277  RNA, variant U1 small nuclear 19
AliasesRNU1-126; RNU1-147; RNVU1-13; vU1.13; 
vU1.19
GeneCards (Weizmann)RNVU1-19
Ensembl hg19 (Hinxton)ENSG00000275538 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275538 [Gene_View]  chr1:120850819-120850985 [Contig_View]  RNVU1-19 [Vega]
ICGC DataPortalENSG00000275538
TCGA cBioPortalRNVU1-19
AceView (NCBI)RNVU1-19
Genatlas (Paris)RNVU1-19
WikiGenes101954277
SOURCE (Princeton)RNVU1-19
Genetics Home Reference (NIH)RNVU1-19
Genomic and cartography
GoldenPath hg38 (UCSC)RNVU1-19  -     chr1:120850819-120850985 -  1p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RNVU1-19  -     1p11.2   [Description]    (hg19-Feb_2009)
EnsemblRNVU1-19 - 1p11.2 [CytoView hg19]  RNVU1-19 - 1p11.2 [CytoView hg38]
Mapping of homologs : NCBIRNVU1-19 [Mapview hg19]  RNVU1-19 [Mapview hg38]
Gene and transcription
Genbank (Entrez)JQ988807
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RNVU1-19
Alternative Splicing GalleryENSG00000275538
Gene ExpressionRNVU1-19 [ NCBI-GEO ]   RNVU1-19 [ EBI - ARRAY_EXPRESS ]   RNVU1-19 [ SEEK ]   RNVU1-19 [ MEM ]
Gene Expression Viewer (FireBrowse)RNVU1-19 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101954277
GTEX Portal (Tissue expression)RNVU1-19
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)RNVU1-19
DMDM Disease mutations101954277
Blocks (Seattle)RNVU1-19
Human Protein AtlasENSG00000275538
Protein Interaction databases
FunCoupENSG00000275538
BioGRIDRNVU1-19
STRING (EMBL)RNVU1-19
ZODIACRNVU1-19
Ontologies - Pathways
Huge Navigator RNVU1-19 [HugePedia]
snp3D : Map Gene to Disease101954277
BioCentury BCIQRNVU1-19
ClinGenRNVU1-19
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101954277
Clinical trialRNVU1-19
Miscellaneous
canSAR (ICR)RNVU1-19 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRNVU1-19
EVEXRNVU1-19
GoPubMedRNVU1-19
iHOPRNVU1-19
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 11:51:24 CEST 2017

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