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GVQW3 (GVQW motif containing 3)

Identity

Other alias-
HGNC (Hugo) GVQW3
LocusID (NCBI) 100506127
Atlas_Id 80578
Location 11q13.5  [Link to chromosome band 11q13]
Location_base_pair Starts at 76381303 and ends at 76408131 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


External links

Nomenclature
HGNC (Hugo)GVQW3   51239
Cards
Entrez_Gene (NCBI)GVQW3  100506127  GVQW motif containing 3
Aliases
GeneCards (Weizmann)GVQW3
Ensembl hg19 (Hinxton)ENSG00000179240 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000179240 [Gene_View]  ENSG00000179240 [Sequence]  chr11:76381303-76408131 [Contig_View]  GVQW3 [Vega]
ICGC DataPortalENSG00000179240
TCGA cBioPortalGVQW3
AceView (NCBI)GVQW3
Genatlas (Paris)GVQW3
WikiGenes100506127
SOURCE (Princeton)GVQW3
Genetics Home Reference (NIH)GVQW3
Genomic and cartography
GoldenPath hg38 (UCSC)GVQW3  -     chr11:76381303-76408131 +  11q13.5   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GVQW3  -     11q13.5   [Description]    (hg19-Feb_2009)
GoldenPathGVQW3 - 11q13.5 [CytoView hg19]  GVQW3 - 11q13.5 [CytoView hg38]
ImmunoBaseENSG00000179240
Mapping of homologs : NCBIGVQW3 [Mapview hg19]  GVQW3 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI289296 AK054952 AK095089 AK125821 BC040665
RefSeq transcript (Entrez)NM_001013634 NM_001282456 NM_001305225 NM_001347884 NM_001347885
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GVQW3
Cluster EST : UnigeneHs.734014 [ NCBI ]
CGAP (NCI)Hs.734014
Alternative Splicing GalleryENSG00000179240
Gene ExpressionGVQW3 [ NCBI-GEO ]   GVQW3 [ EBI - ARRAY_EXPRESS ]   GVQW3 [ SEEK ]   GVQW3 [ MEM ]
Gene Expression Viewer (FireBrowse)GVQW3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100506127
GTEX Portal (Tissue expression)GVQW3
Human Protein AtlasENSG00000179240-GVQW3 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ3ZCU0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ3ZCU0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ3ZCU0
Splice isoforms : SwissVarQ3ZCU0
PhosPhoSitePlusQ3ZCU0
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GVQW3
DMDM Disease mutations100506127
Blocks (Seattle)GVQW3
SuperfamilyQ3ZCU0
Human Protein Atlas [tissue]ENSG00000179240-GVQW3 [tissue]
Peptide AtlasQ3ZCU0
IPIIPI00651646   IPI00759461   IPI00982269   
Protein Interaction databases
DIP (DOE-UCLA)Q3ZCU0
IntAct (EBI)Q3ZCU0
FunCoupENSG00000179240
BioGRIDGVQW3
STRING (EMBL)GVQW3
ZODIACGVQW3
Ontologies - Pathways
QuickGOQ3ZCU0
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkGVQW3
Atlas of Cancer Signalling NetworkGVQW3
Wikipedia pathwaysGVQW3
Orthology - Evolution
OrthoDB100506127
GeneTree (enSembl)ENSG00000179240
Phylogenetic Trees/Animal Genes : TreeFamGVQW3
HOGENOMQ3ZCU0
Homologs : HomoloGeneGVQW3
Homology/Alignments : Family Browser (UCSC)GVQW3
Gene fusions - Rearrangements
Fusion : QuiverGVQW3
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGVQW3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GVQW3
dbVarGVQW3
ClinVarGVQW3
1000_GenomesGVQW3 
Exome Variant ServerGVQW3
ExAC (Exome Aggregation Consortium)ENSG00000179240
GNOMAD BrowserENSG00000179240
Varsome BrowserGVQW3
Genetic variants : HAPMAP100506127
Genomic Variants (DGV)GVQW3 [DGVbeta]
DECIPHERGVQW3 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGVQW3 
Mutations
ICGC Data PortalGVQW3 
TCGA Data PortalGVQW3 
Broad Tumor PortalGVQW3
OASIS PortalGVQW3 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDGVQW3
BioMutasearch GVQW3
DgiDB (Drug Gene Interaction Database)GVQW3
DoCM (Curated mutations)GVQW3 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GVQW3 (select a term)
intoGenGVQW3
Cancer3DGVQW3(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETGVQW3
MedgenGVQW3
Genetic Testing Registry GVQW3
NextProtQ3ZCU0 [Medical]
TSGene100506127
GENETestsGVQW3
Target ValidationGVQW3
Huge Navigator GVQW3 [HugePedia]
snp3D : Map Gene to Disease100506127
BioCentury BCIQGVQW3
ClinGenGVQW3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506127
Clinical trialGVQW3
Miscellaneous
canSAR (ICR)GVQW3 (select the gene name)
DataMed IndexGVQW3
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGVQW3
EVEXGVQW3
GoPubMedGVQW3
iHOPGVQW3
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Sep 3 15:30:39 CEST 2019

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