Atlas of Genetics and Cytogenetics in Oncology and Haematology

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MRO (maestro)

Identity

Alias (NCBI)B29
C18orf3
HGNC (Hugo) MRO
HGNC Alias symbB29
FLJ30140
HGNC Alias nameB29 protein
 beside the Ma29 deletion
HGNC Previous nameC18orf3
HGNC Previous namechromosome 18 open reading frame 3
LocusID (NCBI) 83876
Atlas_Id 70420
Location 18q21.2  [Link to chromosome band 18q21]
Location_base_pair Starts at 50795120 and ends at 50820064 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)
MRO (18q21.2) / RORA (15q22.2)MRO (18q21.2) / SLC1A2 (11p13)SUPT6H (17q11.2) / MRO (18q21.2)

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

 

Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]
  t(17;18)(q11;q21) SUPT6H/MRO

External links

Nomenclature
HGNC (Hugo)MRO   24121
Cards
Entrez_Gene (NCBI)MRO    maestro
AliasesB29; C18orf3
GeneCards (Weizmann)MRO
Ensembl hg19 (Hinxton)ENSG00000134042 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000134042 [Gene_View]  ENSG00000134042 [Sequence]  chr18:50795120-50820064 [Contig_View]  MRO [Vega]
ICGC DataPortalENSG00000134042
TCGA cBioPortalMRO
AceView (NCBI)MRO
Genatlas (Paris)MRO
SOURCE (Princeton)MRO
Genetics Home Reference (NIH)MRO
Genomic and cartography
GoldenPath hg38 (UCSC)MRO  -     chr18:50795120-50820064 -  18q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MRO  -     18q21.2   [Description]    (hg19-Feb_2009)
GoldenPathMRO - 18q21.2 [CytoView hg19]  MRO - 18q21.2 [CytoView hg38]
ImmunoBaseENSG00000134042
genome Data Viewer NCBIMRO [Mapview hg19]  
OMIM608080   
Gene and transcription
Genbank (Entrez)AB042647 AI479272 AI829586 AK054702 AK294757
RefSeq transcript (Entrez)NM_001127174 NM_001127175 NM_001127176 NM_001369508 NM_001369510 NM_001369511 NM_001369515 NM_031939
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MRO
Alternative Splicing GalleryENSG00000134042
Gene ExpressionMRO [ NCBI-GEO ]   MRO [ EBI - ARRAY_EXPRESS ]   MRO [ SEEK ]   MRO [ MEM ]
Gene Expression Viewer (FireBrowse)MRO [ Firebrowse - Broad ]
GenevisibleExpression of MRO in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)83876
GTEX Portal (Tissue expression)MRO
Human Protein AtlasENSG00000134042-MRO [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9BYG7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9BYG7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9BYG7
Splice isoforms : SwissVarQ9BYG7
PhosPhoSitePlusQ9BYG7
Domains : Interpro (EBI)ARM-type_fold   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MRO
Blocks (Seattle)MRO
SuperfamilyQ9BYG7
Human Protein Atlas [tissue]ENSG00000134042-MRO [tissue]
Peptide AtlasQ9BYG7
HPRD16276
IPIIPI00550876   IPI00643875   IPI00895823   IPI00895893   
Protein Interaction databases
DIP (DOE-UCLA)Q9BYG7
IntAct (EBI)Q9BYG7
BioGRIDMRO
STRING (EMBL)MRO
ZODIACMRO
Ontologies - Pathways
QuickGOQ9BYG7
Ontology : AmiGOnucleolus  
Ontology : EGO-EBInucleolus  
NDEx NetworkMRO
Atlas of Cancer Signalling NetworkMRO
Wikipedia pathwaysMRO
Orthology - Evolution
OrthoDB83876
GeneTree (enSembl)ENSG00000134042
Phylogenetic Trees/Animal Genes : TreeFamMRO
HOGENOMQ9BYG7
Homologs : HomoloGeneMRO
Homology/Alignments : Family Browser (UCSC)MRO
Gene fusions - Rearrangements
Fusion : QuiverMRO
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMRO [hg38]
dbVarMRO
ClinVarMRO
MonarchMRO
1000_GenomesMRO 
Exome Variant ServerMRO
GNOMAD BrowserENSG00000134042
Varsome BrowserMRO
Genomic Variants (DGV)MRO [DGVbeta]
DECIPHERMRO [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMRO 
Mutations
ICGC Data PortalMRO 
TCGA Data PortalMRO 
Broad Tumor PortalMRO
OASIS PortalMRO [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMRO  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMRO
Mutations and Diseases : HGMDMRO
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 MRO
DgiDB (Drug Gene Interaction Database)MRO
DoCM (Curated mutations)MRO (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MRO (select a term)
intoGenMRO
Cancer3DMRO(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM608080   
Orphanet
DisGeNETMRO
MedgenMRO
Genetic Testing Registry MRO
NextProtQ9BYG7 [Medical]
GENETestsMRO
Target ValidationMRO
Huge Navigator MRO [HugePedia]
ClinGenMRO
Clinical trials, drugs, therapy
MyCancerGenomeMRO
Protein Interactions : CTD
Pharm GKB GenePA134932281
Clinical trialMRO
Miscellaneous
canSAR (ICR)MRO (select the gene name)
HarmonizomeMRO
DataMed IndexMRO
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMRO
EVEXMRO
GoPubMedMRO
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Dec 5 17:17:54 CET 2020
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