ENSG00000125414


Homo sapiens

Features
Gene ID: ENSG00000125414
  
Biological name :MYH2
  
Synonyms : MYH2 / myosin heavy chain 2 / Q9UKX2
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: -1
Band: p13.1
Gene start: 10521148
Gene end: 10549957
  
Corresponding Affymetrix probe sets: 204631_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000245503
Ensembl peptide - ENSP00000433944
Ensembl peptide - ENSP00000482463
Ensembl peptide - ENSP00000463668
Ensembl peptide - ENSP00000380367
Ensembl peptide - ENSP00000399348
NCBI entrez gene - 4620     See in Manteia.
OMIM - 160740
RefSeq - NM_017534
RefSeq - NM_001100112
RefSeq Peptide - NP_001093582
RefSeq Peptide - NP_060004
swissprot - Q9UKX2
swissprot - E7EX84
swissprot - J3QLR0
Ensembl - ENSG00000125414
  
Related genetic diseases (OMIM): 605637 - Proximal myopathy and ophthalmoplegia, 605637
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 CABZ01079179.1ENSDARG00000110596Danio rerio
 myhbENSDARG00000001993Danio rerio
 myhz1.1ENSDARG00000102414Danio rerio
 myhz1.3ENSDARG00000067997Danio rerio
 myhz2ENSDARG00000012944Danio rerio
 zgc:66156ENSDARG00000112287Danio rerio
 MYH1AENSGALG00000037864Gallus gallus
 MYH1BENSGALG00000039977Gallus gallus
 MYH1CENSGALG00000032404Gallus gallus
 MYH1DENSGALG00000027323Gallus gallus
 MYH1FENSGALG00000042257Gallus gallus
 MYH1GENSGALG00000028612Gallus gallus
 Myh2ENSMUSG00000033196Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
MYH1 / P12882 / myosin heavy chain 1ENSG0000010906195
MYH8 / P13535 / myosin heavy chain 8ENSG0000013302093
MYH4 / Q9Y623 / myosin heavy chain 4ENSG0000026442492
MYH3 / P11055 / myosin heavy chain 3ENSG0000010906385
MYH13 / Q9UKX3 / myosin heavy chain 13ENSG0000000678882
MYH7 / P12883 / myosin heavy chain 7ENSG0000009205481
MYH6 / P13533 / myosin heavy chain 6ENSG0000019761680
MYH7B / A7E2Y1 / myosin heavy chain 7BENSG0000007881468
MYH15 / Q9Y2K3 / myosin heavy chain 15ENSG0000014482160
MYH11 / P35749 / myosin heavy chain 11ENSG0000013339241
MYH10 / P35580 / myosin heavy chain 10ENSG0000013302640
MYH9 / P35579 / myosin heavy chain 9ENSG0000010034540
MYH14 / Q7Z406 / myosin heavy chain 14ENSG0000010535738


Protein motifs (from Interpro)
Interpro ID Name
 IPR000048  IQ motif, EF-hand binding site
 IPR001609  Myosin head, motor domain
 IPR002928  Myosin tail
 IPR004009  Myosin, N-terminal, SH3-like
 IPR008989  Myosin S1 fragment, N-terminal
 IPR027417  P-loop containing nucleoside triphosphate hydrolase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001778 plasma membrane repair IEA
 biological_processGO:0006936 muscle contraction TAS
 biological_processGO:0007018 microtubule-based movement IEA
 biological_processGO:0014823 response to activity IEA
 biological_processGO:0030049 muscle filament sliding NAS
 biological_processGO:0038096 Fc-gamma receptor signaling pathway involved in phagocytosis TAS
 biological_processGO:0070252 actin-mediated cell contraction IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005794 Golgi apparatus IEA
 cellular_componentGO:0005826 actomyosin contractile ring IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005859 muscle myosin complex TAS
 cellular_componentGO:0005911 cell-cell junction IEA
 cellular_componentGO:0016459 myosin complex IEA
 cellular_componentGO:0030016 myofibril IDA
 cellular_componentGO:0030017 sarcomere NAS
 cellular_componentGO:0031672 A band IEA
 cellular_componentGO:0032982 myosin filament IEA
 cellular_componentGO:0032991 protein-containing complex IDA
 molecular_functionGO:0000146 microfilament motor activity TAS
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003774 motor activity IEA
 molecular_functionGO:0003777 microtubule motor activity IEA
 molecular_functionGO:0003779 actin binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005516 calmodulin binding IEA
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0008017 microtubule binding IEA
 molecular_functionGO:0051015 actin filament binding IEA


Pathways (from Reactome)
Pathway description
Regulation of actin dynamics for phagocytic cup formation


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000218 High palate "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428]
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 HP:0000467 Neck muscle weakness 
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 HP:0000508 Ptosis "Drooping of the eyelid." [HPO:curators]
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 HP:0002058 Myopathic facies "A facial appearance characteristic of myopathic conditions. The face appears expressionless with sunken cheeks, bilateral ptosis, and inability to elevate the corners of the mouth, due to muscle weakness." [HPO:curators]
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 HP:0002460 Distal muscle weakness "Reduced strength of the distal musculature." [HPO:curators]
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 HP:0002515 Waddling gait 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002803 Congenital contractures 
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 HP:0003198 Myopathy 
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 HP:0003324 Generalized muscle weakness "Generalized weakness or decreased strength of the muscles." [HPO:curators]
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 HP:0003691 Scapular winging 
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 HP:0003701 Proximal muscle weakness "A lack of strength of the proximal muscles." [HPO:curators]
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 HP:0003828 Variable expressivity 
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 HP:0100299 Muscle fiber inclusion bodies 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000075624 ACTB / P60709 / actin beta  / complex
 ENSG00000184009 ACTG1 / P63261 / actin gamma 1  / complex






 

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