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MYOZ3 (myozenin 3)

Identity

Alias_symbol (synonym)CS-3
CS3
FRP3
Other alias
HGNC (Hugo) MYOZ3
LocusID (NCBI) 91977
Atlas_Id 50952
Location 5q33.1  [Link to chromosome band 5q33]
Location_base_pair Starts at 150040403 and ends at 150058930 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)MYOZ3   18565
Cards
Entrez_Gene (NCBI)MYOZ3  91977  myozenin 3
AliasesCS-3; CS3; FRP3
GeneCards (Weizmann)MYOZ3
Ensembl hg19 (Hinxton)ENSG00000164591 [Gene_View]  chr5:150040403-150058930 [Contig_View]  MYOZ3 [Vega]
Ensembl hg38 (Hinxton)ENSG00000164591 [Gene_View]  chr5:150040403-150058930 [Contig_View]  MYOZ3 [Vega]
ICGC DataPortalENSG00000164591
TCGA cBioPortalMYOZ3
AceView (NCBI)MYOZ3
Genatlas (Paris)MYOZ3
WikiGenes91977
SOURCE (Princeton)MYOZ3
Genetics Home Reference (NIH)MYOZ3
Genomic and cartography
GoldenPath hg19 (UCSC)MYOZ3  -     chr5:150040403-150058930 +  5q33.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MYOZ3  -     5q33.1   [Description]    (hg38-Dec_2013)
EnsemblMYOZ3 - 5q33.1 [CytoView hg19]  MYOZ3 - 5q33.1 [CytoView hg38]
Mapping of homologs : NCBIMYOZ3 [Mapview hg19]  MYOZ3 [Mapview hg38]
OMIM610735   
Gene and transcription
Genbank (Entrez)AA969304 AF052497 AF480443 AJ277961 AJ300586
RefSeq transcript (Entrez)NM_001122853 NM_133371
RefSeq genomic (Entrez)NC_000005 NC_018916 NG_032584 NT_029289 NW_004929324
Consensus coding sequences : CCDS (NCBI)MYOZ3
Cluster EST : UnigeneHs.91626 [ NCBI ]
CGAP (NCI)Hs.91626
Alternative Splicing GalleryENSG00000164591
Gene ExpressionMYOZ3 [ NCBI-GEO ]   MYOZ3 [ EBI - ARRAY_EXPRESS ]   MYOZ3 [ SEEK ]   MYOZ3 [ MEM ]
Gene Expression Viewer (FireBrowse)MYOZ3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)91977
GTEX Portal (Tissue expression)MYOZ3
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TDC0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TDC0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TDC0
Splice isoforms : SwissVarQ8TDC0
PhosPhoSitePlusQ8TDC0
Domains : Interpro (EBI)MYOZ   
Domain families : Pfam (Sanger)Calsarcin (PF05556)   
Domain families : Pfam (NCBI)pfam05556   
Conserved Domain (NCBI)MYOZ3
DMDM Disease mutations91977
Blocks (Seattle)MYOZ3
SuperfamilyQ8TDC0
Human Protein AtlasENSG00000164591
Peptide AtlasQ8TDC0
HPRD17624
IPIIPI00152507   IPI00383424   IPI00642599   IPI00979083   IPI00973877   
Protein Interaction databases
DIP (DOE-UCLA)Q8TDC0
IntAct (EBI)Q8TDC0
FunCoupENSG00000164591
BioGRIDMYOZ3
STRING (EMBL)MYOZ3
ZODIACMYOZ3
Ontologies - Pathways
QuickGOQ8TDC0
Ontology : AmiGOprotein binding  Z disc  
Ontology : EGO-EBIprotein binding  Z disc  
NDEx NetworkMYOZ3
Atlas of Cancer Signalling NetworkMYOZ3
Wikipedia pathwaysMYOZ3
Orthology - Evolution
OrthoDB91977
GeneTree (enSembl)ENSG00000164591
Phylogenetic Trees/Animal Genes : TreeFamMYOZ3
HOVERGENQ8TDC0
HOGENOMQ8TDC0
Homologs : HomoloGeneMYOZ3
Homology/Alignments : Family Browser (UCSC)MYOZ3
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMYOZ3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MYOZ3
dbVarMYOZ3
ClinVarMYOZ3
1000_GenomesMYOZ3 
Exome Variant ServerMYOZ3
ExAC (Exome Aggregation Consortium)MYOZ3 (select the gene name)
Genetic variants : HAPMAP91977
Genomic Variants (DGV)MYOZ3 [DGVbeta]
DECIPHER (Syndromes)5:150040403-150058930  ENSG00000164591
CONAN: Copy Number AnalysisMYOZ3 
Mutations
ICGC Data PortalMYOZ3 
TCGA Data PortalMYOZ3 
Broad Tumor PortalMYOZ3
OASIS PortalMYOZ3 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMYOZ3  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMYOZ3
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)Leiden Muscular Dystrophy pages
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MYOZ3
DgiDB (Drug Gene Interaction Database)MYOZ3
DoCM (Curated mutations)MYOZ3 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MYOZ3 (select a term)
intoGenMYOZ3
Cancer3DMYOZ3(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM610735   
Orphanet
MedgenMYOZ3
Genetic Testing Registry MYOZ3
NextProtQ8TDC0 [Medical]
TSGene91977
GENETestsMYOZ3
Huge Navigator MYOZ3 [HugePedia]
snp3D : Map Gene to Disease91977
BioCentury BCIQMYOZ3
ClinGenMYOZ3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD91977
Chemical/Pharm GKB GenePA38577
Clinical trialMYOZ3
Miscellaneous
canSAR (ICR)MYOZ3 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMYOZ3
EVEXMYOZ3
GoPubMedMYOZ3
iHOPMYOZ3
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 13:17:58 CET 2017

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