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VENTX (VENT homeobox)

Identity

Alias_namesVENTX2
VENT-like homeobox 2
VENT homeobox homolog (Xenopus laevis)
Alias_symbol (synonym)HPX42B
Other aliasNA88A
HGNC (Hugo) VENTX
LocusID (NCBI) 27287
Atlas_Id 42790
Location 10q26.3  [Link to chromosome band 10q26]
Location_base_pair Starts at 135051408 and ends at 135055434 bp from pter ( according to hg19-Feb_2009)

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)VENTX   13639
Cards
Entrez_Gene (NCBI)VENTX  27287  VENT homeobox
AliasesHPX42B; NA88A; VENTX2
GeneCards (Weizmann)VENTX
Ensembl hg19 (Hinxton)ENSG00000151650 [Gene_View]  chr10:135051408-135055434 [Contig_View]  VENTX [Vega]
Ensembl hg38 (Hinxton)ENSG00000151650 [Gene_View]  chr10:135051408-135055434 [Contig_View]  VENTX [Vega]
ICGC DataPortalENSG00000151650
TCGA cBioPortalVENTX
AceView (NCBI)VENTX
Genatlas (Paris)VENTX
WikiGenes27287
SOURCE (Princeton)VENTX
Genetics Home Reference (NIH)VENTX
Genomic and cartography
GoldenPath hg19 (UCSC)VENTX  -     chr10:135051408-135055434 +  10q26.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)VENTX  -     10q26.3   [Description]    (hg38-Dec_2013)
EnsemblVENTX - 10q26.3 [CytoView hg19]  VENTX - 10q26.3 [CytoView hg38]
Mapping of homologs : NCBIVENTX [Mapview hg19]  VENTX [Mapview hg38]
OMIM607158   
Gene and transcription
Genbank (Entrez)AF068006 BC108915 BC108916 BX089390 CA390754
RefSeq transcript (Entrez)NM_014468
RefSeq genomic (Entrez)NC_000010 NC_018921 NT_030059 NW_004929377
Consensus coding sequences : CCDS (NCBI)VENTX
Cluster EST : UnigeneHs.125231 [ NCBI ]
CGAP (NCI)Hs.125231
Alternative Splicing GalleryENSG00000151650
Gene ExpressionVENTX [ NCBI-GEO ]   VENTX [ EBI - ARRAY_EXPRESS ]   VENTX [ SEEK ]   VENTX [ MEM ]
Gene Expression Viewer (FireBrowse)VENTX [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)27287
GTEX Portal (Tissue expression)VENTX
Protein : pattern, domain, 3D structure
UniProt/SwissProtO95231   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO95231  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO95231
Splice isoforms : SwissVarO95231
PhosPhoSitePlusO95231
Domaine pattern : Prosite (Expaxy)HOMEOBOX_1 (PS00027)    HOMEOBOX_2 (PS50071)   
Domains : Interpro (EBI)Homeobox_CS    Homeobox_dom    Homeodomain-like   
Domain families : Pfam (Sanger)Homeobox (PF00046)   
Domain families : Pfam (NCBI)pfam00046   
Domain families : Smart (EMBL)HOX (SM00389)  
Conserved Domain (NCBI)VENTX
DMDM Disease mutations27287
Blocks (Seattle)VENTX
SuperfamilyO95231
Human Protein AtlasENSG00000151650
Peptide AtlasO95231
HPRD06197
IPIIPI00004447   
Protein Interaction databases
DIP (DOE-UCLA)O95231
IntAct (EBI)O95231
FunCoupENSG00000151650
BioGRIDVENTX
STRING (EMBL)VENTX
ZODIACVENTX
Ontologies - Pathways
QuickGOO95231
Ontology : AmiGOprotein binding  nucleus  regulation of transcription, DNA-templated  multicellular organism development  sequence-specific DNA binding  
Ontology : EGO-EBIprotein binding  nucleus  regulation of transcription, DNA-templated  multicellular organism development  sequence-specific DNA binding  
NDEx NetworkVENTX
Atlas of Cancer Signalling NetworkVENTX
Wikipedia pathwaysVENTX
Orthology - Evolution
OrthoDB27287
GeneTree (enSembl)ENSG00000151650
Phylogenetic Trees/Animal Genes : TreeFamVENTX
HOVERGENO95231
HOGENOMO95231
Homologs : HomoloGeneVENTX
Homology/Alignments : Family Browser (UCSC)VENTX
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerVENTX [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)VENTX
dbVarVENTX
ClinVarVENTX
1000_GenomesVENTX 
Exome Variant ServerVENTX
ExAC (Exome Aggregation Consortium)VENTX (select the gene name)
Genetic variants : HAPMAP27287
Genomic Variants (DGV)VENTX [DGVbeta]
DECIPHER (Syndromes)10:135051408-135055434  ENSG00000151650
CONAN: Copy Number AnalysisVENTX 
Mutations
ICGC Data PortalVENTX 
TCGA Data PortalVENTX 
Broad Tumor PortalVENTX
OASIS PortalVENTX [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICVENTX  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDVENTX
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch VENTX
DgiDB (Drug Gene Interaction Database)VENTX
DoCM (Curated mutations)VENTX (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)VENTX (select a term)
intoGenVENTX
Cancer3DVENTX(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607158   
Orphanet
MedgenVENTX
Genetic Testing Registry VENTX
NextProtO95231 [Medical]
TSGene27287
GENETestsVENTX
Huge Navigator VENTX [HugePedia]
snp3D : Map Gene to Disease27287
BioCentury BCIQVENTX
ClinGenVENTX
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD27287
Chemical/Pharm GKB GenePA37803
Clinical trialVENTX
Miscellaneous
canSAR (ICR)VENTX (select the gene name)
Probes
Litterature
PubMed14 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineVENTX
EVEXVENTX
GoPubMedVENTX
iHOPVENTX
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Mar 30 15:24:44 CEST 2017

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