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MROH8 (maestro heat like repeat family member 8)

Identity

Alias_namesC20orf131
C20orf132
chromosome 20 open reading frame 131
chromosome 20 open reading frame 132
maestro heat-like repeat family member 8
Alias_symbol (synonym)dJ621N11.4
dJ621N11.3
Other alias
HGNC (Hugo) MROH8
LocusID (NCBI) 140699
Atlas_Id 70429
Location 20q11.23  [Link to chromosome band 20q11]
Location_base_pair Starts at 37101226 and ends at 37179588 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)
ADNP (20q13.13) / MROH8 (20q11.23)EVA1C (21q22.11) / MROH8 (20q11.23)

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)MROH8   16125
Cards
Entrez_Gene (NCBI)MROH8  140699  maestro heat like repeat family member 8
AliasesC20orf131; C20orf132; dJ621N11.3; dJ621N11.4
GeneCards (Weizmann)MROH8
Ensembl hg19 (Hinxton)ENSG00000101353 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000101353 [Gene_View]  chr20:37101226-37179588 [Contig_View]  MROH8 [Vega]
ICGC DataPortalENSG00000101353
TCGA cBioPortalMROH8
AceView (NCBI)MROH8
Genatlas (Paris)MROH8
WikiGenes140699
SOURCE (Princeton)MROH8
Genetics Home Reference (NIH)MROH8
Genomic and cartography
GoldenPath hg38 (UCSC)MROH8  -     chr20:37101226-37179588 -  20q11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MROH8  -     20q11.23   [Description]    (hg19-Feb_2009)
EnsemblMROH8 - 20q11.23 [CytoView hg19]  MROH8 - 20q11.23 [CytoView hg38]
Mapping of homologs : NCBIMROH8 [Mapview hg19]  MROH8 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093432 AL833864 AL844420 AM392522 AM392819
RefSeq transcript (Entrez)NM_152503 NM_213631 NM_213632
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MROH8
Cluster EST : UnigeneHs.349125 [ NCBI ]
CGAP (NCI)Hs.349125
Alternative Splicing GalleryENSG00000101353
Gene ExpressionMROH8 [ NCBI-GEO ]   MROH8 [ EBI - ARRAY_EXPRESS ]   MROH8 [ SEEK ]   MROH8 [ MEM ]
Gene Expression Viewer (FireBrowse)MROH8 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)140699
GTEX Portal (Tissue expression)MROH8
Human Protein AtlasENSG00000101353-MROH8 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H579   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H579  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H579
Splice isoforms : SwissVarQ9H579
PhosPhoSitePlusQ9H579
Domains : Interpro (EBI)ARM-type_fold   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MROH8
DMDM Disease mutations140699
Blocks (Seattle)MROH8
SuperfamilyQ9H579
Human Protein Atlas [tissue]ENSG00000101353-MROH8 [tissue]
Peptide AtlasQ9H579
HPRD12745
IPIIPI00477327   IPI01009603   IPI00218635   IPI00419281   IPI00220372   IPI00829732   IPI00829660   
Protein Interaction databases
DIP (DOE-UCLA)Q9H579
IntAct (EBI)Q9H579
FunCoupENSG00000101353
BioGRIDMROH8
STRING (EMBL)MROH8
ZODIACMROH8
Ontologies - Pathways
QuickGOQ9H579
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkMROH8
Atlas of Cancer Signalling NetworkMROH8
Wikipedia pathwaysMROH8
Orthology - Evolution
OrthoDB140699
GeneTree (enSembl)ENSG00000101353
Phylogenetic Trees/Animal Genes : TreeFamMROH8
HOVERGENQ9H579
HOGENOMQ9H579
Homologs : HomoloGeneMROH8
Homology/Alignments : Family Browser (UCSC)MROH8
Gene fusions - Rearrangements
Tumor Fusion PortalMROH8
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMROH8 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MROH8
dbVarMROH8
ClinVarMROH8
1000_GenomesMROH8 
Exome Variant ServerMROH8
ExAC (Exome Aggregation Consortium)ENSG00000101353
GNOMAD BrowserENSG00000101353
Genetic variants : HAPMAP140699
Genomic Variants (DGV)MROH8 [DGVbeta]
DECIPHERMROH8 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMROH8 
Mutations
ICGC Data PortalMROH8 
TCGA Data PortalMROH8 
Broad Tumor PortalMROH8
OASIS PortalMROH8 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMROH8
BioMutasearch MROH8
DgiDB (Drug Gene Interaction Database)MROH8
DoCM (Curated mutations)MROH8 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MROH8 (select a term)
intoGenMROH8
Cancer3DMROH8(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMROH8
MedgenMROH8
Genetic Testing Registry MROH8
NextProtQ9H579 [Medical]
TSGene140699
GENETestsMROH8
Target ValidationMROH8
Huge Navigator MROH8 [HugePedia]
snp3D : Map Gene to Disease140699
BioCentury BCIQMROH8
ClinGenMROH8
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD140699
Chemical/Pharm GKB GenePA25674
Clinical trialMROH8
Miscellaneous
canSAR (ICR)MROH8 (select the gene name)
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMROH8
EVEXMROH8
GoPubMedMROH8
iHOPMROH8
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 13:41:59 CET 2017

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