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RHOV (ras homolog family member V)

Identity

Alias (NCBI)ARHV
CHP
WRCH2
HGNC (Hugo) RHOV
HGNC Alias symbChp
WRCH2
HGNC Previous nameARHV
HGNC Previous nameras homolog gene family, member V
LocusID (NCBI) 171177
Atlas_Id 53970
Location 15q15.1  [Link to chromosome band 15q15]
Location_base_pair Starts at 40872214 and ends at 40874234 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)RHOV   18313
Cards
Entrez_Gene (NCBI)RHOV    ras homolog family member V
AliasesARHV; CHP; WRCH2
GeneCards (Weizmann)RHOV
Ensembl hg19 (Hinxton)ENSG00000104140 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000104140 [Gene_View]  ENSG00000104140 [Sequence]  chr15:40872214-40874234 [Contig_View]  RHOV [Vega]
ICGC DataPortalENSG00000104140
TCGA cBioPortalRHOV
AceView (NCBI)RHOV
Genatlas (Paris)RHOV
SOURCE (Princeton)RHOV
Genetics Home Reference (NIH)RHOV
Genomic and cartography
GoldenPath hg38 (UCSC)RHOV  -     chr15:40872214-40874234 -  15q15.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RHOV  -     15q15.1   [Description]    (hg19-Feb_2009)
GoldenPathRHOV - 15q15.1 [CytoView hg19]  RHOV - 15q15.1 [CytoView hg38]
ImmunoBaseENSG00000104140
Genome Data Viewer NCBIRHOV [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AB079131 AY059636 BC019353 BC105020 BC105022
RefSeq transcript (Entrez)NM_133639
Consensus coding sequences : CCDS (NCBI)RHOV
Gene ExpressionRHOV [ NCBI-GEO ]   RHOV [ EBI - ARRAY_EXPRESS ]   RHOV [ SEEK ]   RHOV [ MEM ]
Gene Expression Viewer (FireBrowse)RHOV [ Firebrowse - Broad ]
GenevisibleExpression of RHOV in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)171177
GTEX Portal (Tissue expression)RHOV
Human Protein AtlasENSG00000104140-RHOV [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96L33   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96L33  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96L33
PhosPhoSitePlusQ96L33
Domaine pattern : Prosite (Expaxy)RHO (PS51420)   
Domains : Interpro (EBI)P-loop_NTPase    Small_GTP-bd_dom    Small_GTPase    Small_GTPase_Rho   
Domain families : Pfam (Sanger)Ras (PF00071)   
Domain families : Pfam (NCBI)pfam00071   
Conserved Domain (NCBI)RHOV
SuperfamilyQ96L33
AlphaFold pdb e-kbQ96L33   
Human Protein Atlas [tissue]ENSG00000104140-RHOV [tissue]
HPRD10191
Protein Interaction databases
DIP (DOE-UCLA)Q96L33
IntAct (EBI)Q96L33
BioGRIDRHOV
STRING (EMBL)RHOV
ZODIACRHOV
Ontologies - Pathways
QuickGOQ96L33
Ontology : AmiGOGTPase activity  protein binding  GTP binding  cytosol  plasma membrane  endocytosis  endosome membrane  cell migration  cell projection assembly  Cdc42 protein signal transduction  metal ion binding  regulation of small GTPase mediated signal transduction  
Ontology : EGO-EBIGTPase activity  protein binding  GTP binding  cytosol  plasma membrane  endocytosis  endosome membrane  cell migration  cell projection assembly  Cdc42 protein signal transduction  metal ion binding  regulation of small GTPase mediated signal transduction  
NDEx NetworkRHOV
Atlas of Cancer Signalling NetworkRHOV
Wikipedia pathwaysRHOV
Orthology - Evolution
OrthoDB171177
GeneTree (enSembl)ENSG00000104140
Phylogenetic Trees/Animal Genes : TreeFamRHOV
Homologs : HomoloGeneRHOV
Homology/Alignments : Family Browser (UCSC)RHOV
Gene fusions - Rearrangements
Fusion : QuiverRHOV
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerRHOV [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)RHOV
dbVarRHOV
ClinVarRHOV
MonarchRHOV
1000_GenomesRHOV 
Exome Variant ServerRHOV
GNOMAD BrowserENSG00000104140
Varsome BrowserRHOV
ACMGRHOV variants
VarityQ96L33
Genomic Variants (DGV)RHOV [DGVbeta]
DECIPHERRHOV [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisRHOV 
Mutations
ICGC Data PortalRHOV 
TCGA Data PortalRHOV 
Broad Tumor PortalRHOV
OASIS PortalRHOV [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICRHOV  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DRHOV
Mutations and Diseases : HGMDRHOV
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaRHOV
DgiDB (Drug Gene Interaction Database)RHOV
DoCM (Curated mutations)RHOV
CIViC (Clinical Interpretations of Variants in Cancer)RHOV
Cancer3DRHOV
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETRHOV
MedgenRHOV
Genetic Testing Registry RHOV
NextProtQ96L33 [Medical]
GENETestsRHOV
Target ValidationRHOV
Huge Navigator RHOV [HugePedia]
ClinGenRHOV
Clinical trials, drugs, therapy
MyCancerGenomeRHOV
Protein Interactions : CTDRHOV
Pharm GKB GenePA38313
PharosQ96L33
Clinical trialRHOV
Miscellaneous
canSAR (ICR)RHOV
HarmonizomeRHOV
DataMed IndexRHOV
Probes
Litterature
PubMed17 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXRHOV
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:28:57 CEST 2021

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