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MYOM2 (myomesin 2)

Identity

Alias (NCBI)TTNAP
HGNC (Hugo) MYOM2
HGNC Previous namemyomesin (M-protein) 2 (165kD)
 myomesin (M-protein) 2, 165kDa
LocusID (NCBI) 9172
Atlas_Id 41484
Location 8p23.3  [Link to chromosome band 8p23]
Location_base_pair Starts at 2045046 and ends at 2145456 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)
HNRNPK (9q21.32) / MYOM2 (8p23.3)

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)MYOM2   7614
Cards
Entrez_Gene (NCBI)MYOM2    myomesin 2
AliasesTTNAP
GeneCards (Weizmann)MYOM2
Ensembl hg19 (Hinxton)ENSG00000036448 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000036448 [Gene_View]  ENSG00000036448 [Sequence]  chr8:2045046-2145456 [Contig_View]  MYOM2 [Vega]
ICGC DataPortalENSG00000036448
TCGA cBioPortalMYOM2
AceView (NCBI)MYOM2
Genatlas (Paris)MYOM2
SOURCE (Princeton)MYOM2
Genetics Home Reference (NIH)MYOM2
Genomic and cartography
GoldenPath hg38 (UCSC)MYOM2  -     chr8:2045046-2145456 +  8p23.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MYOM2  -     8p23.3   [Description]    (hg19-Feb_2009)
GoldenPathMYOM2 - 8p23.3 [CytoView hg19]  MYOM2 - 8p23.3 [CytoView hg38]
ImmunoBaseENSG00000036448
Genome Data Viewer NCBIMYOM2 [Mapview hg19]  
OMIM603509   
Gene and transcription
Genbank (Entrez)AJ708170 AK297890 AL596730 BC052969 BM720057
RefSeq transcript (Entrez)NM_003970
Consensus coding sequences : CCDS (NCBI)MYOM2
Gene ExpressionMYOM2 [ NCBI-GEO ]   MYOM2 [ EBI - ARRAY_EXPRESS ]   MYOM2 [ SEEK ]   MYOM2 [ MEM ]
Gene Expression Viewer (FireBrowse)MYOM2 [ Firebrowse - Broad ]
GenevisibleExpression of MYOM2 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9172
GTEX Portal (Tissue expression)MYOM2
Human Protein AtlasENSG00000036448-MYOM2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP54296   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP54296  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP54296
PhosPhoSitePlusP54296
Domaine pattern : Prosite (Expaxy)FN3 (PS50853)    IG_LIKE (PS50835)   
Domains : Interpro (EBI)FN3_dom    FN3_sf    Ig-like_dom    Ig-like_dom_sf    Ig-like_fold    Ig_I-set    Ig_sub    Ig_sub2   
Domain families : Pfam (Sanger)fn3 (PF00041)    I-set (PF07679)   
Domain families : Pfam (NCBI)pfam00041    pfam07679   
Domain families : Smart (EMBL)FN3 (SM00060)  IG (SM00409)  IGc2 (SM00408)  
Conserved Domain (NCBI)MYOM2
SuperfamilyP54296
AlphaFold pdb e-kbP54296   
Human Protein Atlas [tissue]ENSG00000036448-MYOM2 [tissue]
HPRD04619
Protein Interaction databases
DIP (DOE-UCLA)P54296
IntAct (EBI)P54296
BioGRIDMYOM2
STRING (EMBL)MYOM2
ZODIACMYOM2
Ontologies - Pathways
QuickGOP54296
Ontology : AmiGOextraocular skeletal muscle development  protein binding  mitochondrion  muscle contraction  structural constituent of muscle  kinase binding  M band  myosin filament  sarcomere organization  actin filament binding  
Ontology : EGO-EBIextraocular skeletal muscle development  protein binding  mitochondrion  muscle contraction  structural constituent of muscle  kinase binding  M band  myosin filament  sarcomere organization  actin filament binding  
NDEx NetworkMYOM2
Atlas of Cancer Signalling NetworkMYOM2
Wikipedia pathwaysMYOM2
Orthology - Evolution
OrthoDB9172
GeneTree (enSembl)ENSG00000036448
Phylogenetic Trees/Animal Genes : TreeFamMYOM2
Homologs : HomoloGeneMYOM2
Homology/Alignments : Family Browser (UCSC)MYOM2
Gene fusions - Rearrangements
Fusion : QuiverMYOM2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMYOM2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MYOM2
dbVarMYOM2
ClinVarMYOM2
MonarchMYOM2
1000_GenomesMYOM2 
Exome Variant ServerMYOM2
GNOMAD BrowserENSG00000036448
Varsome BrowserMYOM2
ACMGMYOM2 variants
VarityP54296
Genomic Variants (DGV)MYOM2 [DGVbeta]
DECIPHERMYOM2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMYOM2 
Mutations
ICGC Data PortalMYOM2 
TCGA Data PortalMYOM2 
Broad Tumor PortalMYOM2
OASIS PortalMYOM2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMYOM2  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMYOM2
Mutations and Diseases : HGMDMYOM2
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMYOM2
DgiDB (Drug Gene Interaction Database)MYOM2
DoCM (Curated mutations)MYOM2
CIViC (Clinical Interpretations of Variants in Cancer)MYOM2
Cancer3DMYOM2
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM603509   
Orphanet
DisGeNETMYOM2
MedgenMYOM2
Genetic Testing Registry MYOM2
NextProtP54296 [Medical]
GENETestsMYOM2
Target ValidationMYOM2
Huge Navigator MYOM2 [HugePedia]
ClinGenMYOM2
Clinical trials, drugs, therapy
MyCancerGenomeMYOM2
Protein Interactions : CTDMYOM2
Pharm GKB GenePA31419
PharosP54296
Clinical trialMYOM2
Miscellaneous
canSAR (ICR)MYOM2
HarmonizomeMYOM2
DataMed IndexMYOM2
Probes
Litterature
PubMed22 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMYOM2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:21:53 CEST 2021

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