Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIOS (meiosis regulator for oocyte development)

Identity

Alias_namesmissing oocyte, meiosis regulator, homolog (Drosophila)
missing oocyte meiosis regulator homolog
Alias_symbol (synonym)FLJ20323
MIO
Sea4
Other alias
HGNC (Hugo) MIOS
LocusID (NCBI) 54468
Atlas_Id 68992
Location 7p21.3  [Link to chromosome band 7p21]
Location_base_pair Starts at 7566985 and ends at 7607479 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)
MIOS (7p21.3) / ADAP1 (7p22.3)

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)MIOS   21905
Cards
Entrez_Gene (NCBI)MIOS  54468  meiosis regulator for oocyte development
AliasesMIO; Sea4
GeneCards (Weizmann)MIOS
Ensembl hg19 (Hinxton)ENSG00000164654 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000164654 [Gene_View]  chr7:7566985-7607479 [Contig_View]  MIOS [Vega]
ICGC DataPortalENSG00000164654
TCGA cBioPortalMIOS
AceView (NCBI)MIOS
Genatlas (Paris)MIOS
WikiGenes54468
SOURCE (Princeton)MIOS
Genetics Home Reference (NIH)MIOS
Genomic and cartography
GoldenPath hg38 (UCSC)MIOS  -     chr7:7566985-7607479 +  7p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIOS  -     7p21.3   [Description]    (hg19-Feb_2009)
EnsemblMIOS - 7p21.3 [CytoView hg19]  MIOS - 7p21.3 [CytoView hg38]
Mapping of homologs : NCBIMIOS [Mapview hg19]  MIOS [Mapview hg38]
OMIM615359   
Gene and transcription
Genbank (Entrez)AK000330 AK096829 AK294561 AL136892 BC005883
RefSeq transcript (Entrez)NM_019005
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIOS
Cluster EST : UnigeneHs.520215 [ NCBI ]
CGAP (NCI)Hs.520215
Alternative Splicing GalleryENSG00000164654
Gene ExpressionMIOS [ NCBI-GEO ]   MIOS [ EBI - ARRAY_EXPRESS ]   MIOS [ SEEK ]   MIOS [ MEM ]
Gene Expression Viewer (FireBrowse)MIOS [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)54468
GTEX Portal (Tissue expression)MIOS
Human Protein AtlasENSG00000164654-MIOS [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NXC5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NXC5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NXC5
Splice isoforms : SwissVarQ9NXC5
PhosPhoSitePlusQ9NXC5
Domains : Interpro (EBI)WD40/YVTN_repeat-like_dom    WD40_repeat    WD40_repeat_dom    Zn_ribbon_mio   
Domain families : Pfam (Sanger)zinc_ribbon_16 (PF17034)   
Domain families : Pfam (NCBI)pfam17034   
Domain families : Smart (EMBL)WD40 (SM00320)  
Conserved Domain (NCBI)MIOS
DMDM Disease mutations54468
Blocks (Seattle)MIOS
SuperfamilyQ9NXC5
Human Protein Atlas [tissue]ENSG00000164654-MIOS [tissue]
Peptide AtlasQ9NXC5
HPRD07898
IPIIPI00301987   IPI00889558   IPI01011739   IPI00894444   IPI00894219   
Protein Interaction databases
DIP (DOE-UCLA)Q9NXC5
IntAct (EBI)Q9NXC5
FunCoupENSG00000164654
BioGRIDMIOS
STRING (EMBL)MIOS
ZODIACMIOS
Ontologies - Pathways
QuickGOQ9NXC5
Ontology : AmiGOprotein binding  lysosomal membrane  positive regulation of TOR signaling  cellular response to amino acid starvation  cellular protein complex localization  GATOR2 complex  
Ontology : EGO-EBIprotein binding  lysosomal membrane  positive regulation of TOR signaling  cellular response to amino acid starvation  cellular protein complex localization  GATOR2 complex  
NDEx NetworkMIOS
Atlas of Cancer Signalling NetworkMIOS
Wikipedia pathwaysMIOS
Orthology - Evolution
OrthoDB54468
GeneTree (enSembl)ENSG00000164654
Phylogenetic Trees/Animal Genes : TreeFamMIOS
HOVERGENQ9NXC5
HOGENOMQ9NXC5
Homologs : HomoloGeneMIOS
Homology/Alignments : Family Browser (UCSC)MIOS
Gene fusions - Rearrangements
Tumor Fusion PortalMIOS
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMIOS [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MIOS
dbVarMIOS
ClinVarMIOS
1000_GenomesMIOS 
Exome Variant ServerMIOS
ExAC (Exome Aggregation Consortium)ENSG00000164654
GNOMAD BrowserENSG00000164654
Genetic variants : HAPMAP54468
Genomic Variants (DGV)MIOS [DGVbeta]
DECIPHERMIOS [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMIOS 
Mutations
ICGC Data PortalMIOS 
TCGA Data PortalMIOS 
Broad Tumor PortalMIOS
OASIS PortalMIOS [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMIOS  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMIOS
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 MIOS
DgiDB (Drug Gene Interaction Database)MIOS
DoCM (Curated mutations)MIOS (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MIOS (select a term)
intoGenMIOS
Cancer3DMIOS(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM615359   
Orphanet
DisGeNETMIOS
MedgenMIOS
Genetic Testing Registry MIOS
NextProtQ9NXC5 [Medical]
TSGene54468
GENETestsMIOS
Target ValidationMIOS
Huge Navigator MIOS [HugePedia]
snp3D : Map Gene to Disease54468
BioCentury BCIQMIOS
ClinGenMIOS
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD54468
Chemical/Pharm GKB GenePA164722300
Clinical trialMIOS
Miscellaneous
canSAR (ICR)MIOS (select the gene name)
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIOS
EVEXMIOS
GoPubMedMIOS
iHOPMIOS
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Nov 20 19:56:38 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.