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

MOSMO (modulator of smoothened)

Identity

Other aliasATTHOG
BC030336
C16orf52
HGNC (Hugo) MOSMO
LocusID (NCBI) 730094
Atlas_Id 80481
Location 16p12.2  [Link to chromosome band 16p12]
Location_base_pair Starts at 22008135 and ends at 22084651 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)
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


External links

Nomenclature
HGNC (Hugo)MOSMO   27087
Cards
Entrez_Gene (NCBI)MOSMO  730094  modulator of smoothened
AliasesATTHOG; BC030336; C16orf52
GeneCards (Weizmann)MOSMO
Ensembl hg19 (Hinxton)ENSG00000185716 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000185716 [Gene_View]  ENSG00000185716 [Sequence]  chr16:22008135-22084651 [Contig_View]  MOSMO [Vega]
ICGC DataPortalENSG00000185716
TCGA cBioPortalMOSMO
AceView (NCBI)MOSMO
Genatlas (Paris)MOSMO
WikiGenes730094
SOURCE (Princeton)MOSMO
Genetics Home Reference (NIH)MOSMO
Genomic and cartography
GoldenPath hg38 (UCSC)MOSMO  -     chr16:22008135-22084651 +  16p12.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MOSMO  -     16p12.2   [Description]    (hg19-Feb_2009)
GoldenPathMOSMO - 16p12.2 [CytoView hg19]  MOSMO - 16p12.2 [CytoView hg38]
ImmunoBaseENSG00000185716
genome Data Viewer NCBIMOSMO [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AF086142 AK095585 AK310438 BC027604 BC045557
RefSeq transcript (Entrez)NM_001164579 NM_173501
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MOSMO
Alternative Splicing GalleryENSG00000185716
Gene ExpressionMOSMO [ NCBI-GEO ]   MOSMO [ EBI - ARRAY_EXPRESS ]   MOSMO [ SEEK ]   MOSMO [ MEM ]
Gene Expression Viewer (FireBrowse)MOSMO [ Firebrowse - Broad ]
GenevisibleExpression of MOSMO in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)730094
GTEX Portal (Tissue expression)MOSMO
Human Protein AtlasENSG00000185716-MOSMO [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NHV5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NHV5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NHV5
Splice isoforms : SwissVarQ8NHV5
PhosPhoSitePlusQ8NHV5
Domains : Interpro (EBI)Mosmo   
Domain families : Pfam (Sanger)Atthog (PF18800)   
Domain families : Pfam (NCBI)pfam18800   
Conserved Domain (NCBI)MOSMO
DMDM Disease mutations730094
Blocks (Seattle)MOSMO
SuperfamilyQ8NHV5
Human Protein Atlas [tissue]ENSG00000185716-MOSMO [tissue]
Peptide AtlasQ8NHV5
IPIIPI00816379   IPI00169347   
Protein Interaction databases
DIP (DOE-UCLA)Q8NHV5
IntAct (EBI)Q8NHV5
FunCoupENSG00000185716
BioGRIDMOSMO
STRING (EMBL)MOSMO
ZODIACMOSMO
Ontologies - Pathways
QuickGOQ8NHV5
Ontology : AmiGOGolgi apparatus  Golgi apparatus  plasma membrane  integral component of membrane  regulation of protein stability  regulation of neuron differentiation  negative regulation of smoothened signaling pathway  negative regulation of smoothened signaling pathway  ciliary membrane  ciliary membrane  
Ontology : EGO-EBIGolgi apparatus  Golgi apparatus  plasma membrane  integral component of membrane  regulation of protein stability  regulation of neuron differentiation  negative regulation of smoothened signaling pathway  negative regulation of smoothened signaling pathway  ciliary membrane  ciliary membrane  
NDEx NetworkMOSMO
Atlas of Cancer Signalling NetworkMOSMO
Wikipedia pathwaysMOSMO
Orthology - Evolution
OrthoDB730094
GeneTree (enSembl)ENSG00000185716
Phylogenetic Trees/Animal Genes : TreeFamMOSMO
HOGENOMQ8NHV5
Homologs : HomoloGeneMOSMO
Homology/Alignments : Family Browser (UCSC)MOSMO
Gene fusions - Rearrangements
Fusion : QuiverMOSMO
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMOSMO [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MOSMO
dbVarMOSMO
ClinVarMOSMO
1000_GenomesMOSMO 
Exome Variant ServerMOSMO
GNOMAD BrowserENSG00000185716
Varsome BrowserMOSMO
Genetic variants : HAPMAP730094
Genomic Variants (DGV)MOSMO [DGVbeta]
DECIPHERMOSMO [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMOSMO 
Mutations
ICGC Data PortalMOSMO 
TCGA Data PortalMOSMO 
Broad Tumor PortalMOSMO
OASIS PortalMOSMO [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMOSMO  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMOSMO
Mutations and Diseases : HGMDMOSMO
BioMutasearch MOSMO
DgiDB (Drug Gene Interaction Database)MOSMO
DoCM (Curated mutations)MOSMO (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MOSMO (select a term)
intoGenMOSMO
Cancer3DMOSMO(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMOSMO
MedgenMOSMO
Genetic Testing Registry MOSMO
NextProtQ8NHV5 [Medical]
TSGene730094
GENETestsMOSMO
Target ValidationMOSMO
Huge Navigator MOSMO [HugePedia]
snp3D : Map Gene to Disease730094
BioCentury BCIQMOSMO
ClinGenMOSMO
Clinical trials, drugs, therapy
Protein Interactions : CTD730094
Pharm GKB GenePA142672259
Clinical trialMOSMO
Miscellaneous
canSAR (ICR)MOSMO (select the gene name)
HarmonizomeMOSMO
DataMed IndexMOSMO
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMOSMO
EVEXMOSMO
GoPubMedMOSMO
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 : Fri Jul 10 20:26:33 CEST 2020

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.