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ART5 (ADP-ribosyltransferase 5)

Identity

Other aliasARTC5
HGNC (Hugo) ART5
LocusID (NCBI) 116969
Atlas_Id 60542
Location 11p15.4  [Link to chromosome band 11p15]
Location_base_pair Starts at 3638506 and ends at 3642316 bp from pter ( according to hg38-Dec_2013)

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)ART5   24049
Cards
Entrez_Gene (NCBI)ART5  116969  ADP-ribosyltransferase 5
AliasesARTC5
GeneCards (Weizmann)ART5
Ensembl hg19 (Hinxton)ENSG00000167311 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000167311 [Gene_View]  chr11:3638506-3642316 [Contig_View]  ART5 [Vega]
ICGC DataPortalENSG00000167311
TCGA cBioPortalART5
AceView (NCBI)ART5
Genatlas (Paris)ART5
WikiGenes116969
SOURCE (Princeton)ART5
Genetics Home Reference (NIH)ART5
Genomic and cartography
GoldenPath hg38 (UCSC)ART5  -     chr11:3638506-3642316 -  11p15.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ART5  -     11p15.4   [Description]    (hg19-Feb_2009)
EnsemblART5 - 11p15.4 [CytoView hg19]  ART5 - 11p15.4 [CytoView hg38]
Mapping of homologs : NCBIART5 [Mapview hg19]  ART5 [Mapview hg38]
OMIM610625   
Gene and transcription
Genbank (Entrez)AK313531 AW241897 AY358466 BC014577 BI825352
RefSeq transcript (Entrez)NM_001079536 NM_001297668 NM_053017
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ART5
Cluster EST : UnigeneHs.125680 [ NCBI ]
CGAP (NCI)Hs.125680
Alternative Splicing GalleryENSG00000167311
Gene ExpressionART5 [ NCBI-GEO ]   ART5 [ EBI - ARRAY_EXPRESS ]   ART5 [ SEEK ]   ART5 [ MEM ]
Gene Expression Viewer (FireBrowse)ART5 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)116969
GTEX Portal (Tissue expression)ART5
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96L15   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96L15  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96L15
Splice isoforms : SwissVarQ96L15
Catalytic activity : Enzyme2.4.2.31 [ Enzyme-Expasy ]   2.4.2.312.4.2.31 [ IntEnz-EBI ]   2.4.2.31 [ BRENDA ]   2.4.2.31 [ KEGG ]   
PhosPhoSitePlusQ96L15
Domaine pattern : Prosite (Expaxy)ART (PS01291)   
Domains : Interpro (EBI)ART   
Domain families : Pfam (Sanger)ART (PF01129)   
Domain families : Pfam (NCBI)pfam01129   
Conserved Domain (NCBI)ART5
DMDM Disease mutations116969
Blocks (Seattle)ART5
SuperfamilyQ96L15
Human Protein AtlasENSG00000167311
Peptide AtlasQ96L15
HPRD12493
IPIIPI00432414   IPI00328943   IPI00852756   IPI00853487   
Protein Interaction databases
DIP (DOE-UCLA)Q96L15
IntAct (EBI)Q96L15
FunCoupENSG00000167311
BioGRIDART5
STRING (EMBL)ART5
ZODIACART5
Ontologies - Pathways
QuickGOQ96L15
Ontology : AmiGONAD+ ADP-ribosyltransferase activity  NAD+ nucleosidase activity  NAD(P)+-protein-arginine ADP-ribosyltransferase activity  extracellular region  protein ADP-ribosylation  membrane  
Ontology : EGO-EBINAD+ ADP-ribosyltransferase activity  NAD+ nucleosidase activity  NAD(P)+-protein-arginine ADP-ribosyltransferase activity  extracellular region  protein ADP-ribosylation  membrane  
NDEx NetworkART5
Atlas of Cancer Signalling NetworkART5
Wikipedia pathwaysART5
Orthology - Evolution
OrthoDB116969
GeneTree (enSembl)ENSG00000167311
Phylogenetic Trees/Animal Genes : TreeFamART5
HOVERGENQ96L15
HOGENOMQ96L15
Homologs : HomoloGeneART5
Homology/Alignments : Family Browser (UCSC)ART5
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerART5 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ART5
dbVarART5
ClinVarART5
1000_GenomesART5 
Exome Variant ServerART5
ExAC (Exome Aggregation Consortium)ART5 (select the gene name)
Genetic variants : HAPMAP116969
Genomic Variants (DGV)ART5 [DGVbeta]
DECIPHERART5 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisART5 
Mutations
ICGC Data PortalART5 
TCGA Data PortalART5 
Broad Tumor PortalART5
OASIS PortalART5 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICART5  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDART5
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 ART5
DgiDB (Drug Gene Interaction Database)ART5
DoCM (Curated mutations)ART5 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ART5 (select a term)
intoGenART5
Cancer3DART5(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM610625   
Orphanet
MedgenART5
Genetic Testing Registry ART5
NextProtQ96L15 [Medical]
TSGene116969
GENETestsART5
Huge Navigator ART5 [HugePedia]
snp3D : Map Gene to Disease116969
BioCentury BCIQART5
ClinGenART5
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD116969
Chemical/Pharm GKB GenePA134887713
Clinical trialART5
Miscellaneous
canSAR (ICR)ART5 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineART5
EVEXART5
GoPubMedART5
iHOPART5
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 11:00:58 CEST 2017

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