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MROH9 (maestro heat like repeat family member 9)

Identity

Alias_namesC1orf129
chromosome 1 open reading frame 129
maestro heat-like repeat family member 9
Alias_symbol (synonym)FLJ23550
ARMC11
Other alias
HGNC (Hugo) MROH9
LocusID (NCBI) 80133
Atlas_Id 70430
Location 1q24.3  [Link to chromosome band 1q24]
Location_base_pair Starts at 170935471 and ends at 171064765 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
MROH9 (1q24.3) / RP1-45C12.1 ()NOS1AP (1q23.3) / MROH9 (1q24.3)

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)MROH9   26287
Cards
Entrez_Gene (NCBI)MROH9  80133  maestro heat like repeat family member 9
AliasesARMC11; C1orf129
GeneCards (Weizmann)MROH9
Ensembl hg19 (Hinxton)ENSG00000117501 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000117501 [Gene_View]  chr1:170935471-171064765 [Contig_View]  MROH9 [Vega]
ICGC DataPortalENSG00000117501
TCGA cBioPortalMROH9
AceView (NCBI)MROH9
Genatlas (Paris)MROH9
WikiGenes80133
SOURCE (Princeton)MROH9
Genetics Home Reference (NIH)MROH9
Genomic and cartography
GoldenPath hg38 (UCSC)MROH9  -     chr1:170935471-171064765 +  1q24.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MROH9  -     1q24.3   [Description]    (hg19-Feb_2009)
EnsemblMROH9 - 1q24.3 [CytoView hg19]  MROH9 - 1q24.3 [CytoView hg38]
Mapping of homologs : NCBIMROH9 [Mapview hg19]  MROH9 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK027203 BC113390 BC113392 DB096780 DB211602
RefSeq transcript (Entrez)NM_001163629 NM_025063
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MROH9
Cluster EST : UnigeneHs.591489 [ NCBI ]
CGAP (NCI)Hs.591489
Alternative Splicing GalleryENSG00000117501
Gene ExpressionMROH9 [ NCBI-GEO ]   MROH9 [ EBI - ARRAY_EXPRESS ]   MROH9 [ SEEK ]   MROH9 [ MEM ]
Gene Expression Viewer (FireBrowse)MROH9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)80133
GTEX Portal (Tissue expression)MROH9
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5TGP6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5TGP6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5TGP6
Splice isoforms : SwissVarQ5TGP6
PhosPhoSitePlusQ5TGP6
Domains : Interpro (EBI)ARM-like    ARM-type_fold   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MROH9
DMDM Disease mutations80133
Blocks (Seattle)MROH9
SuperfamilyQ5TGP6
Human Protein AtlasENSG00000117501
Peptide AtlasQ5TGP6
HPRD08672
IPIIPI00017952   IPI00514048   
Protein Interaction databases
DIP (DOE-UCLA)Q5TGP6
IntAct (EBI)Q5TGP6
FunCoupENSG00000117501
BioGRIDMROH9
STRING (EMBL)MROH9
ZODIACMROH9
Ontologies - Pathways
QuickGOQ5TGP6
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkMROH9
Atlas of Cancer Signalling NetworkMROH9
Wikipedia pathwaysMROH9
Orthology - Evolution
OrthoDB80133
GeneTree (enSembl)ENSG00000117501
Phylogenetic Trees/Animal Genes : TreeFamMROH9
HOVERGENQ5TGP6
HOGENOMQ5TGP6
Homologs : HomoloGeneMROH9
Homology/Alignments : Family Browser (UCSC)MROH9
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMROH9 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MROH9
dbVarMROH9
ClinVarMROH9
1000_GenomesMROH9 
Exome Variant ServerMROH9
ExAC (Exome Aggregation Consortium)MROH9 (select the gene name)
Genetic variants : HAPMAP80133
Genomic Variants (DGV)MROH9 [DGVbeta]
DECIPHERMROH9 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMROH9 
Mutations
ICGC Data PortalMROH9 
TCGA Data PortalMROH9 
Broad Tumor PortalMROH9
OASIS PortalMROH9 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMROH9
BioMutasearch MROH9
DgiDB (Drug Gene Interaction Database)MROH9
DoCM (Curated mutations)MROH9 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MROH9 (select a term)
intoGenMROH9
Cancer3DMROH9(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMROH9
Genetic Testing Registry MROH9
NextProtQ5TGP6 [Medical]
TSGene80133
GENETestsMROH9
Target ValidationMROH9
Huge Navigator MROH9 [HugePedia]
snp3D : Map Gene to Disease80133
BioCentury BCIQMROH9
ClinGenMROH9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD80133
Chemical/Pharm GKB GenePA142672447
Clinical trialMROH9
Miscellaneous
canSAR (ICR)MROH9 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMROH9
EVEXMROH9
GoPubMedMROH9
iHOPMROH9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:31:25 CEST 2017

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