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MINOS1 (mitochondrial inner membrane organizing system 1)

Identity

Alias_namesC1orf151
chromosome 1 open reading frame 151
Alias_symbol (synonym)RP5-1056L3.2
FLJ36999
MIO10
Mic10
Other alias
HGNC (Hugo) MINOS1
LocusID (NCBI) 440574
Atlas_Id 54460
Location 1p36.13  [Link to chromosome band 1p36]
Location_base_pair Starts at 19923471 and ends at 19956315 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
BAX (19q13.33) / MINOS1 (1p36.13)MINOS1 (1p36.13) / NPDC1 (9q34.3)MINOS1 (1p36.13) / PTMA (2q37.1)
MINOS1 (1p36.13) / QARS (3p21.31)MINOS1 (1p36.13) / RCC2 (1p36.13)

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)MINOS1   32068
Cards
Entrez_Gene (NCBI)MINOS1  440574  mitochondrial inner membrane organizing system 1
AliasesC1orf151; MIO10; Mic10
GeneCards (Weizmann)MINOS1
Ensembl hg19 (Hinxton)ENSG00000173436 [Gene_View]  chr1:19923471-19956315 [Contig_View]  MINOS1 [Vega]
Ensembl hg38 (Hinxton)ENSG00000173436 [Gene_View]  chr1:19923471-19956315 [Contig_View]  MINOS1 [Vega]
ICGC DataPortalENSG00000173436
TCGA cBioPortalMINOS1
AceView (NCBI)MINOS1
Genatlas (Paris)MINOS1
WikiGenes440574
SOURCE (Princeton)MINOS1
Genetics Home Reference (NIH)MINOS1
Genomic and cartography
GoldenPath hg19 (UCSC)MINOS1  -     chr1:19923471-19956315 +  1p36.13   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MINOS1  -     1p36.13   [Description]    (hg38-Dec_2013)
EnsemblMINOS1 - 1p36.13 [CytoView hg19]  MINOS1 - 1p36.13 [CytoView hg38]
Mapping of homologs : NCBIMINOS1 [Mapview hg19]  MINOS1 [Mapview hg38]
OMIM616574   
Gene and transcription
Genbank (Entrez)AJ711911 AK094318 AK096240 BC009927 BC070388
RefSeq transcript (Entrez)NM_001032363 NM_001204082 NM_001204083
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929289
Consensus coding sequences : CCDS (NCBI)MINOS1
Cluster EST : UnigeneHs.466662 [ NCBI ]
CGAP (NCI)Hs.466662
Alternative Splicing GalleryENSG00000173436
Gene ExpressionMINOS1 [ NCBI-GEO ]   MINOS1 [ EBI - ARRAY_EXPRESS ]   MINOS1 [ SEEK ]   MINOS1 [ MEM ]
Gene Expression Viewer (FireBrowse)MINOS1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)440574
GTEX Portal (Tissue expression)MINOS1
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5TGZ0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5TGZ0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5TGZ0
Splice isoforms : SwissVarQ5TGZ0
PhosPhoSitePlusQ5TGZ0
Domains : Interpro (EBI)DUF543   
Domain families : Pfam (Sanger)DUF543 (PF04418)   
Domain families : Pfam (NCBI)pfam04418   
Conserved Domain (NCBI)MINOS1
DMDM Disease mutations440574
Blocks (Seattle)MINOS1
SuperfamilyQ5TGZ0
Human Protein AtlasENSG00000173436
Peptide AtlasQ5TGZ0
IPIIPI00062298   IPI00816419   IPI00978529   IPI00977644   
Protein Interaction databases
DIP (DOE-UCLA)Q5TGZ0
IntAct (EBI)Q5TGZ0
FunCoupENSG00000173436
BioGRIDMINOS1
STRING (EMBL)MINOS1
ZODIACMINOS1
Ontologies - Pathways
QuickGOQ5TGZ0
Ontology : AmiGOmolecular_function  protein binding  mitochondrion  mitochondrial inner membrane  biological_process  integral component of membrane  
Ontology : EGO-EBImolecular_function  protein binding  mitochondrion  mitochondrial inner membrane  biological_process  integral component of membrane  
NDEx NetworkMINOS1
Atlas of Cancer Signalling NetworkMINOS1
Wikipedia pathwaysMINOS1
Orthology - Evolution
OrthoDB440574
GeneTree (enSembl)ENSG00000173436
Phylogenetic Trees/Animal Genes : TreeFamMINOS1
HOVERGENQ5TGZ0
HOGENOMQ5TGZ0
Homologs : HomoloGeneMINOS1
Homology/Alignments : Family Browser (UCSC)MINOS1
Gene fusions - Rearrangements
Fusion : MitelmanMINOS1/RCC2 [1p36.13/1p36.13]  
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMINOS1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MINOS1
dbVarMINOS1
ClinVarMINOS1
1000_GenomesMINOS1 
Exome Variant ServerMINOS1
ExAC (Exome Aggregation Consortium)MINOS1 (select the gene name)
Genetic variants : HAPMAP440574
Genomic Variants (DGV)MINOS1 [DGVbeta]
DECIPHER (Syndromes)1:19923471-19956315  ENSG00000173436
CONAN: Copy Number AnalysisMINOS1 
Mutations
ICGC Data PortalMINOS1 
TCGA Data PortalMINOS1 
Broad Tumor PortalMINOS1
OASIS PortalMINOS1 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMINOS1
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MINOS1
DgiDB (Drug Gene Interaction Database)MINOS1
DoCM (Curated mutations)MINOS1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MINOS1 (select a term)
intoGenMINOS1
Cancer3DMINOS1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM616574   
Orphanet
MedgenMINOS1
Genetic Testing Registry MINOS1
NextProtQ5TGZ0 [Medical]
TSGene440574
GENETestsMINOS1
Huge Navigator MINOS1 [HugePedia]
snp3D : Map Gene to Disease440574
BioCentury BCIQMINOS1
ClinGenMINOS1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD440574
Chemical/Pharm GKB GenePA142672468
Clinical trialMINOS1
Miscellaneous
canSAR (ICR)MINOS1 (select the gene name)
Probes
Litterature
PubMed18 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMINOS1
EVEXMINOS1
GoPubMedMINOS1
iHOPMINOS1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 13:15:14 CET 2017

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