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RNVU1-7 (RNA, variant U1 small nuclear 7)

Identity

Alias_namesRNU1-9
RNU1-9P
RNVU1-9
RNU1-6P
RNU1-26P
RNA, U1 small nuclear 9
RNA, U1 small nuclear 9, pseudogene
RNA, variant U1 small nuclear 9
RNA, U1 small nuclear 6, pseudogene
RNA, U1 small nuclear 26, pseudogene
Alias_symbol (synonym)vU1.7
vU1.9
Other aliasRNU1-6
HGNC (Hugo) RNVU1-7
LocusID (NCBI) 26864
Atlas_Id 79899
Location 1q21.2  [Link to chromosome band 1q21]
Location_base_pair Starts at 148038753 and ends at 148038916 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)RNVU1-7   37500
Cards
Entrez_Gene (NCBI)RNVU1-7  26864  RNA, variant U1 small nuclear 7
AliasesRNU1-26P; RNU1-6; RNU1-6P; RNU1-9; 
RNU1-9P; RNVU1-9; vU1.7; vU1.9
GeneCards (Weizmann)RNVU1-7
Ensembl hg19 (Hinxton)ENSG00000206585 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000206585 [Gene_View]  chr1:148038753-148038916 [Contig_View]  RNVU1-7 [Vega]
ICGC DataPortalENSG00000206585
TCGA cBioPortalRNVU1-7
AceView (NCBI)RNVU1-7
Genatlas (Paris)RNVU1-7
WikiGenes26864
SOURCE (Princeton)RNVU1-7
Genetics Home Reference (NIH)RNVU1-7
Genomic and cartography
GoldenPath hg38 (UCSC)RNVU1-7  -     chr1:148038753-148038916 -  1q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RNVU1-7  -     1q21.2   [Description]    (hg19-Feb_2009)
EnsemblRNVU1-7 - 1q21.2 [CytoView hg19]  RNVU1-7 - 1q21.2 [CytoView hg38]
Mapping of homologs : NCBIRNVU1-7 [Mapview hg19]  RNVU1-7 [Mapview hg38]
Gene and transcription
Genbank (Entrez)JQ988801 JQ988803
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RNVU1-7
Alternative Splicing GalleryENSG00000206585
Gene ExpressionRNVU1-7 [ NCBI-GEO ]   RNVU1-7 [ EBI - ARRAY_EXPRESS ]   RNVU1-7 [ SEEK ]   RNVU1-7 [ MEM ]
Gene Expression Viewer (FireBrowse)RNVU1-7 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)26864
GTEX Portal (Tissue expression)RNVU1-7
Human Protein AtlasENSG00000206585-RNVU1-7 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)RNVU1-7
DMDM Disease mutations26864
Blocks (Seattle)RNVU1-7
Human Protein Atlas [tissue]ENSG00000206585-RNVU1-7 [tissue]
Protein Interaction databases
FunCoupENSG00000206585
BioGRIDRNVU1-7
STRING (EMBL)RNVU1-7
ZODIACRNVU1-7
Ontologies - Pathways
Huge Navigator RNVU1-7 [HugePedia]
snp3D : Map Gene to Disease26864
BioCentury BCIQRNVU1-7
ClinGenRNVU1-7
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD26864
Chemical/Pharm GKB GenePA34495
Clinical trialRNVU1-7
Miscellaneous
canSAR (ICR)RNVU1-7 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRNVU1-7
EVEXRNVU1-7
GoPubMedRNVU1-7
iHOPRNVU1-7
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 13:02:42 CET 2017

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