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PRMT3 (protein arginine methyltransferase 3)

Identity

Alias_namesHRMT1L3
HMT1 hnRNP methyltransferase-like 3 (S. cerevisiae)
Other alias
HGNC (Hugo) PRMT3
LocusID (NCBI) 10196
Atlas_Id 46415
Location 11p15.1  [Link to chromosome band 11p15]
Location_base_pair Starts at 20409076 and ends at 20530879 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
SBF2 (11p15.4) / PRMT3 (11p15.1)UPF3A (13q34) / PRMT3 (11p15.1)SBF2 11p15.4 / PRMT3 11p15.1

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)PRMT3   30163
Cards
Entrez_Gene (NCBI)PRMT3  10196  protein arginine methyltransferase 3
AliasesHRMT1L3
GeneCards (Weizmann)PRMT3
Ensembl hg19 (Hinxton)ENSG00000185238 [Gene_View]  chr11:20409076-20530879 [Contig_View]  PRMT3 [Vega]
Ensembl hg38 (Hinxton)ENSG00000185238 [Gene_View]  chr11:20409076-20530879 [Contig_View]  PRMT3 [Vega]
ICGC DataPortalENSG00000185238
TCGA cBioPortalPRMT3
AceView (NCBI)PRMT3
Genatlas (Paris)PRMT3
WikiGenes10196
SOURCE (Princeton)PRMT3
Genetics Home Reference (NIH)PRMT3
Genomic and cartography
GoldenPath hg19 (UCSC)PRMT3  -     chr11:20409076-20530879 +  11p15.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)PRMT3  -     11p15.1   [Description]    (hg38-Dec_2013)
EnsemblPRMT3 - 11p15.1 [CytoView hg19]  PRMT3 - 11p15.1 [CytoView hg38]
Mapping of homologs : NCBIPRMT3 [Mapview hg19]  PRMT3 [Mapview hg38]
OMIM603190   
Gene and transcription
Genbank (Entrez)AF059531 AK125039 AK129984 AK298185 AK300591
RefSeq transcript (Entrez)NM_001145166 NM_001145167 NM_005788
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_009237 NW_004929378
Consensus coding sequences : CCDS (NCBI)PRMT3
Cluster EST : UnigeneHs.152337 [ NCBI ]
CGAP (NCI)Hs.152337
Alternative Splicing GalleryENSG00000185238
Gene ExpressionPRMT3 [ NCBI-GEO ]   PRMT3 [ EBI - ARRAY_EXPRESS ]   PRMT3 [ SEEK ]   PRMT3 [ MEM ]
Gene Expression Viewer (FireBrowse)PRMT3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)10196
GTEX Portal (Tissue expression)PRMT3
Protein : pattern, domain, 3D structure
UniProt/SwissProtO60678   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO60678  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO60678
Splice isoforms : SwissVarO60678
Catalytic activity : Enzyme2.1.1.- [ Enzyme-Expasy ]   2.1.1.-2.1.1.- [ IntEnz-EBI ]   2.1.1.- [ BRENDA ]   2.1.1.- [ KEGG ]   
PhosPhoSitePlusO60678
Domaine pattern : Prosite (Expaxy)SAM_MT_PRMT (PS51678)    ZINC_FINGER_C2H2_1 (PS00028)   
Domains : Interpro (EBI)Arg_MeTrfase    SAM-dependent_MTases    Znf_C2H2    Znf_C2H2-like   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)PRMT3
DMDM Disease mutations10196
Blocks (Seattle)PRMT3
PDB (SRS)2FYT    3SMQ    4HSG    4QQN    4RYL   
PDB (PDBSum)2FYT    3SMQ    4HSG    4QQN    4RYL   
PDB (IMB)2FYT    3SMQ    4HSG    4QQN    4RYL   
PDB (RSDB)2FYT    3SMQ    4HSG    4QQN    4RYL   
Structural Biology KnowledgeBase2FYT    3SMQ    4HSG    4QQN    4RYL   
SCOP (Structural Classification of Proteins)2FYT    3SMQ    4HSG    4QQN    4RYL   
CATH (Classification of proteins structures)2FYT    3SMQ    4HSG    4QQN    4RYL   
SuperfamilyO60678
Human Protein AtlasENSG00000185238
Peptide AtlasO60678
HPRD11934
IPIIPI00401321   IPI00909714   IPI01012872   IPI00922411   IPI00973921   IPI00984385   
Protein Interaction databases
DIP (DOE-UCLA)O60678
IntAct (EBI)O60678
FunCoupENSG00000185238
BioGRIDPRMT3
STRING (EMBL)PRMT3
ZODIACPRMT3
Ontologies - Pathways
QuickGOO60678
Ontology : AmiGOprotein binding  cytoplasm  cytosol  ribosome  regulation of transcription, DNA-templated  methyltransferase activity  histone-arginine N-methyltransferase activity  protein-arginine N-methyltransferase activity  peptidyl-arginine methylation, to asymmetrical-dimethyl arginine  negative regulation of protein ubiquitination  histone arginine methylation  protein-arginine omega-N asymmetric methyltransferase activity  metal ion binding  
Ontology : EGO-EBIprotein binding  cytoplasm  cytosol  ribosome  regulation of transcription, DNA-templated  methyltransferase activity  histone-arginine N-methyltransferase activity  protein-arginine N-methyltransferase activity  peptidyl-arginine methylation, to asymmetrical-dimethyl arginine  negative regulation of protein ubiquitination  histone arginine methylation  protein-arginine omega-N asymmetric methyltransferase activity  metal ion binding  
NDEx NetworkPRMT3
Atlas of Cancer Signalling NetworkPRMT3
Wikipedia pathwaysPRMT3
Orthology - Evolution
OrthoDB10196
GeneTree (enSembl)ENSG00000185238
Phylogenetic Trees/Animal Genes : TreeFamPRMT3
HOVERGENO60678
HOGENOMO60678
Homologs : HomoloGenePRMT3
Homology/Alignments : Family Browser (UCSC)PRMT3
Gene fusions - Rearrangements
Fusion : MitelmanSBF2/PRMT3 [11p15.4/11p15.1]  [t(11;11)(p15;p15)]  
Fusion: TCGASBF2 11p15.4 PRMT3 11p15.1 LUSC
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPRMT3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PRMT3
dbVarPRMT3
ClinVarPRMT3
1000_GenomesPRMT3 
Exome Variant ServerPRMT3
ExAC (Exome Aggregation Consortium)PRMT3 (select the gene name)
Genetic variants : HAPMAP10196
Genomic Variants (DGV)PRMT3 [DGVbeta]
DECIPHER (Syndromes)11:20409076-20530879  ENSG00000185238
CONAN: Copy Number AnalysisPRMT3 
Mutations
ICGC Data PortalPRMT3 
TCGA Data PortalPRMT3 
Broad Tumor PortalPRMT3
OASIS PortalPRMT3 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICPRMT3  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDPRMT3
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 PRMT3
DgiDB (Drug Gene Interaction Database)PRMT3
DoCM (Curated mutations)PRMT3 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PRMT3 (select a term)
intoGenPRMT3
Cancer3DPRMT3(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM603190   
Orphanet
MedgenPRMT3
Genetic Testing Registry PRMT3
NextProtO60678 [Medical]
TSGene10196
GENETestsPRMT3
Huge Navigator PRMT3 [HugePedia]
snp3D : Map Gene to Disease10196
BioCentury BCIQPRMT3
ClinGenPRMT3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD10196
Chemical/Pharm GKB GenePA29462
Clinical trialPRMT3
Miscellaneous
canSAR (ICR)PRMT3 (select the gene name)
Probes
Litterature
PubMed48 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePRMT3
EVEXPRMT3
GoPubMedPRMT3
iHOPPRMT3
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 15:15:44 CEST 2017

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