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RNVU1-14 (RNA, variant U1 small nuclear 14)

Identity

Alias_symbol (synonym)vU1.14
RNU1-37
Other alias
HGNC (Hugo) RNVU1-14
LocusID (NCBI) 101954266
Atlas_Id 78813
Location 1q21.1  [Link to chromosome band 1q21]
Location_base_pair Starts at 145281116 and ends at 145281279 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)RNVU1-14   48319
Cards
Entrez_Gene (NCBI)RNVU1-14  101954266  RNA, variant U1 small nuclear 14
AliasesRNU1-37; vU1.14
GeneCards (Weizmann)RNVU1-14
Ensembl hg19 (Hinxton)ENSG00000207501 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207501 [Gene_View]  chr1:145281116-145281279 [Contig_View]  RNVU1-14 [Vega]
ICGC DataPortalENSG00000207501
TCGA cBioPortalRNVU1-14
AceView (NCBI)RNVU1-14
Genatlas (Paris)RNVU1-14
WikiGenes101954266
SOURCE (Princeton)RNVU1-14
Genetics Home Reference (NIH)RNVU1-14
Genomic and cartography
GoldenPath hg38 (UCSC)RNVU1-14  -     chr1:145281116-145281279 +  1q21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RNVU1-14  -     1q21.1   [Description]    (hg19-Feb_2009)
EnsemblRNVU1-14 - 1q21.1 [CytoView hg19]  RNVU1-14 - 1q21.1 [CytoView hg38]
Mapping of homologs : NCBIRNVU1-14 [Mapview hg19]  RNVU1-14 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RNVU1-14
Alternative Splicing GalleryENSG00000207501
Gene ExpressionRNVU1-14 [ NCBI-GEO ]   RNVU1-14 [ EBI - ARRAY_EXPRESS ]   RNVU1-14 [ SEEK ]   RNVU1-14 [ MEM ]
Gene Expression Viewer (FireBrowse)RNVU1-14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101954266
GTEX Portal (Tissue expression)RNVU1-14
Human Protein AtlasENSG00000207501-RNVU1-14 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)RNVU1-14
DMDM Disease mutations101954266
Blocks (Seattle)RNVU1-14
Human Protein Atlas [tissue]ENSG00000207501-RNVU1-14 [tissue]
Protein Interaction databases
FunCoupENSG00000207501
BioGRIDRNVU1-14
STRING (EMBL)RNVU1-14
ZODIACRNVU1-14
Ontologies - Pathways
Huge Navigator RNVU1-14 [HugePedia]
snp3D : Map Gene to Disease101954266
BioCentury BCIQRNVU1-14
ClinGenRNVU1-14
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101954266
Clinical trialRNVU1-14
Miscellaneous
canSAR (ICR)RNVU1-14 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRNVU1-14
EVEXRNVU1-14
GoPubMedRNVU1-14
iHOPRNVU1-14
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Nov 20 20:10:20 CET 2017

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