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

MOG (myelin oligodendrocyte glycoprotein)

Identity

Alias_symbol (synonym)BTN6
BTNL11
Other aliasMOGIG2
NRCLP7
HGNC (Hugo) MOG
LocusID (NCBI) 4340
Atlas_Id 56532
Location 6p22.1  [Link to chromosome band 6p22]
Location_base_pair Starts at 29656981 and ends at 29672372 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)
MOG (6p22.1) / FBXO7 (22q12.3)MOG (6p22.1) / TTYH2 (17q25.1)

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)MOG   7197
Cards
Entrez_Gene (NCBI)MOG  4340  myelin oligodendrocyte glycoprotein
AliasesBTN6; BTNL11; MOGIG2; NRCLP7
GeneCards (Weizmann)MOG
Ensembl hg19 (Hinxton)ENSG00000204655 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000204655 [Gene_View]  ENSG00000204655 [Sequence]  chr6:29656981-29672372 [Contig_View]  MOG [Vega]
ICGC DataPortalENSG00000204655
TCGA cBioPortalMOG
AceView (NCBI)MOG
Genatlas (Paris)MOG
WikiGenes4340
SOURCE (Princeton)MOG
Genetics Home Reference (NIH)MOG
Genomic and cartography
GoldenPath hg38 (UCSC)MOG  -     chr6:29656981-29672372 +  6p22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MOG  -     6p22.1   [Description]    (hg19-Feb_2009)
EnsemblMOG - 6p22.1 [CytoView hg19]  MOG - 6p22.1 [CytoView hg38]
Mapping of homologs : NCBIMOG [Mapview hg19]  MOG [Mapview hg38]
OMIM159465   614250   
Gene and transcription
Genbank (Entrez)AB209815 AI205181 AK295213 AK308949 AK312892
RefSeq transcript (Entrez)NM_001008228 NM_001008229 NM_001170418 NM_001363610 NM_002433 NM_206809 NM_206810 NM_206811 NM_206812 NM_206813 NM_206814
RefSeq genomic (Entrez)NC_000006 NG_031873 NT_113891 NT_167244 NT_167245 NT_167246 NT_167247 NT_167248 NT_167249
Consensus coding sequences : CCDS (NCBI)MOG
Cluster EST : UnigeneHs.141308 [ NCBI ]
CGAP (NCI)Hs.141308
Alternative Splicing GalleryENSG00000204655
Gene ExpressionMOG [ NCBI-GEO ]   MOG [ EBI - ARRAY_EXPRESS ]   MOG [ SEEK ]   MOG [ MEM ]
Gene Expression Viewer (FireBrowse)MOG [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)4340
GTEX Portal (Tissue expression)MOG
Human Protein AtlasENSG00000204655-MOG [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ16653   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ16653  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ16653
Splice isoforms : SwissVarQ16653
PhosPhoSitePlusQ16653
Domaine pattern : Prosite (Expaxy)IG_LIKE (PS50835)   
Domains : Interpro (EBI)Ig-like_dom    Ig-like_dom_sf    Ig-like_fold    Ig_sub    Ig_V-set    Myelin-oligodendrocyte_glycop   
Domain families : Pfam (Sanger)V-set (PF07686)   
Domain families : Pfam (NCBI)pfam07686   
Domain families : Smart (EMBL)IG (SM00409)  IGv (SM00406)  
Conserved Domain (NCBI)MOG
DMDM Disease mutations4340
Blocks (Seattle)MOG
PDB (SRS)1Q70   
PDB (PDBSum)1Q70   
PDB (IMB)1Q70   
PDB (RSDB)1Q70   
Structural Biology KnowledgeBase1Q70   
SCOP (Structural Classification of Proteins)1Q70   
CATH (Classification of proteins structures)1Q70   
SuperfamilyQ16653
Human Protein Atlas [tissue]ENSG00000204655-MOG [tissue]
Peptide AtlasQ16653
HPRD11831
IPIIPI00556079   IPI00409587   IPI00219664   IPI00943197   IPI00873156   IPI00549656   IPI00953473   IPI00744638   IPI00473134   IPI01021110   IPI00641022   IPI00973501   IPI00973599   IPI00942386   IPI01023052   IPI01022778   IPI00973429   IPI00871600   IPI00643592   IPI00873317   IPI00657941   IPI00973569   IPI00514676   IPI00657666   IPI00927438   IPI00893310   IPI00926497   IPI00893047   IPI00953482   IPI00893938   IPI00945502   IPI00946790   IPI00739655   IPI00945197   
Protein Interaction databases
DIP (DOE-UCLA)Q16653
IntAct (EBI)Q16653
FunCoupENSG00000204655
BioGRIDMOG
STRING (EMBL)MOG
ZODIACMOG
Ontologies - Pathways
QuickGOQ16653
Ontology : AmiGOvirus receptor activity  signaling receptor binding  plasma membrane  cell adhesion  central nervous system development  external side of plasma membrane  integral component of membrane  viral entry into host cell  regulation of immune response  T cell receptor signaling pathway  
Ontology : EGO-EBIvirus receptor activity  signaling receptor binding  plasma membrane  cell adhesion  central nervous system development  external side of plasma membrane  integral component of membrane  viral entry into host cell  regulation of immune response  T cell receptor signaling pathway  
NDEx NetworkMOG
Atlas of Cancer Signalling NetworkMOG
Wikipedia pathwaysMOG
Orthology - Evolution
OrthoDB4340
GeneTree (enSembl)ENSG00000204655
Phylogenetic Trees/Animal Genes : TreeFamMOG
HOVERGENQ16653
HOGENOMQ16653
Homologs : HomoloGeneMOG
Homology/Alignments : Family Browser (UCSC)MOG
Gene fusions - Rearrangements
Fusion : QuiverMOG
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMOG [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MOG
dbVarMOG
ClinVarMOG
1000_GenomesMOG 
Exome Variant ServerMOG
ExAC (Exome Aggregation Consortium)ENSG00000204655
GNOMAD BrowserENSG00000204655
Varsome BrowserMOG
Genetic variants : HAPMAP4340
Genomic Variants (DGV)MOG [DGVbeta]
DECIPHERMOG [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMOG 
Mutations
ICGC Data PortalMOG 
TCGA Data PortalMOG 
Broad Tumor PortalMOG
OASIS PortalMOG [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMOG  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMOG
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 MOG
DgiDB (Drug Gene Interaction Database)MOG
DoCM (Curated mutations)MOG (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MOG (select a term)
intoGenMOG
Cancer3DMOG(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM159465    614250   
Orphanet3637   
DisGeNETMOG
MedgenMOG
Genetic Testing Registry MOG
NextProtQ16653 [Medical]
TSGene4340
GENETestsMOG
Target ValidationMOG
Huge Navigator MOG [HugePedia]
snp3D : Map Gene to Disease4340
BioCentury BCIQMOG
ClinGenMOG
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD4340
Chemical/Pharm GKB GenePA30905
Clinical trialMOG
Miscellaneous
canSAR (ICR)MOG (select the gene name)
Probes
Litterature
PubMed76 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMOG
EVEXMOG
GoPubMedMOG
iHOPMOG
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 : Tue Nov 6 11:23:33 CET 2018

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.