ENSG00000109063


Homo sapiens

Features
Gene ID: ENSG00000109063
  
Biological name :MYH3
  
Synonyms : MYH3 / myosin heavy chain 3 / P11055
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: -1
Band: p13.1
Gene start: 10628526
Gene end: 10657309
  
Corresponding Affymetrix probe sets: 205940_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000464317
NCBI entrez gene - 4621     See in Manteia.
OMIM - 160720
RefSeq - XM_011523871
RefSeq - NM_002470
RefSeq - XM_011523870
RefSeq Peptide - NP_002461
swissprot - P11055
Ensembl - ENSG00000109063
  
Related genetic diseases (OMIM): 178110 - Arthrogryposis, distal, type 8, 178110
  193700 - Arthrogryposis, distal, type 2A, 193700
  601680 - Arthrogryposis, distal, type 2B, 601680
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
 Myh3ENSMUSG00000020908Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
MYH2 / Q9UKX2 / myosin heavy chain 2ENSG0000012541485
MYH1 / P12882 / myosin heavy chain 1ENSG0000010906184
MYH8 / P13535 / myosin heavy chain 8ENSG0000013302084
MYH4 / Q9Y623 / myosin heavy chain 4ENSG0000026442483
MYH6 / P13533 / myosin heavy chain 6ENSG0000019761679
MYH13 / Q9UKX3 / myosin heavy chain 13ENSG0000000678879
MYH7 / P12883 / myosin heavy chain 7ENSG0000009205479
MYH7B / A7E2Y1 / myosin heavy chain 7BENSG0000007881467
MYH15 / Q9Y2K3 / myosin heavy chain 15ENSG0000014482160
MYH11 / P35749 / myosin heavy chain 11ENSG0000013339241
MYH9 / P35579 / myosin heavy chain 9ENSG0000010034541
MYH10 / P35580 / myosin heavy chain 10ENSG0000013302641
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
 IPR036000  Class II myosin, Myh3, motor domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003009 skeletal muscle contraction IMP
 biological_processGO:0006470 protein dephosphorylation IEA
 biological_processGO:0007018 microtubule-based movement IEA
 biological_processGO:0007517 muscle organ development TAS
 biological_processGO:0030048 actin filament-based movement NAS
 biological_processGO:0030049 muscle filament sliding TAS
 biological_processGO:0030326 embryonic limb morphogenesis IC
 biological_processGO:0045214 sarcomere organization NAS
 biological_processGO:0046034 ATP metabolic process IMP
 biological_processGO:0060325 face morphogenesis IC
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0005859 muscle myosin complex NAS
 cellular_componentGO:0016459 myosin complex IEA
 cellular_componentGO:0030016 myofibril IEA
 cellular_componentGO:0030017 sarcomere NAS
 cellular_componentGO:0032982 myosin filament IEA
 cellular_componentGO:0043292 contractile fiber IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0000146 microfilament motor activity IMP
 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 IEA
 molecular_functionGO:0005516 calmodulin binding NAS
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0008017 microtubule binding IEA
 molecular_functionGO:0017018 myosin phosphatase activity TAS
 molecular_functionGO:0042623 ATPase activity, coupled IMP
 molecular_functionGO:0051015 actin filament binding IMP


Pathways (from Reactome)
Pathway description
Striated Muscle Contraction


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:0000023 Inguinal hernia 
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 HP:0000028 Cryptorchidism "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators]
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 HP:0000160 Microstomia "The presence of an abnormally small `mouth` (FMA:49184)." [HPO:curators]
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 HP:0000164 Abnormality of the teeth "Any abnormality of the primary (deciduous) or permanent teeth." [HPO:curators]
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 HP:0000175 Cleft palate "Cleft palate is a developmental defect of the `palate` (FMA:54549) resulting from a failure of fusion of the palatine processes." [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:0000252 Microcephaly "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators]
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 HP:0000272 Malar hypoplasia "Underdeveloped midface region." [HPO:curators]
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 HP:0000275 Narrow face 
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 HP:0000286 Epicanthus "An epicanthal fold is a semilunar fold of skin that extends from the upper eyelid across the medial canthal area to the lower eyelid." [HPO:curators]
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 HP:0000298 Mask-like facies 
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 HP:0000303 Mandibular prognathia "Abnormal prominence of the chin related to an abnormally long mandible." [HPO:curators]
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 HP:0000316 Hypertelorism 
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 HP:0000325 Triangular facies 
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 HP:0000343 Long philtrum 
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 HP:0000346 Whistling Appearance 
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 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
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 HP:0000365 Hearing loss 
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 HP:0000368 Low-set, posteriorly rotated ears 
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 HP:0000411 Protruding ears 
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 HP:0000430 Hypoplastic nasal alae "Thinned, deficient, or excessively arched `ala nasi` (FMA:59519)." [pmid:19152422]
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 HP:0000431 Broad nasal bridge "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators]
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 HP:0000457 Flat nose 
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 HP:0000465 Webbed neck 
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 HP:0000470 Short neck 
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 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
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 HP:0000490 Deep set eyes 
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 HP:0000494 Downward slanting palpebral fissures 
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 HP:0000506 Telecanthus "An abnormally increased distance between the medial canthi (angle between eyelids) of the eyelids." [HPO:curators]
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 HP:0000508 Ptosis "Drooping of the eyelid." [HPO:curators]
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 HP:0000581 Blepharophimosis "Reduced width of the palpebral fissures." [HPO:sdoelken]
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 HP:0000598 Abnormality of the ears 
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 HP:0000951 Abnormality of the skin "An abnormality of the `skin` (FMA:7163)." [HPO:probinson]
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 HP:0001040 Multiple pterygia 
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 HP:0001181 Adducted thumbs 
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 HP:0001193 Ulnar deviation of the hand or of fingers of the hand 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001272 Cerebellar atrophy 
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 HP:0001324 Muscle weakness "Reduced strength of muscles." [HPO:curators]
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 HP:0001363 Craniosynostosis "Craniosynostosis refers to the premature closure of the cranial sutures. Primary craniosynostosis refers to the closure of one or more sutures due to abnormalities in skull development, and secondary craniosynostosis results from failure of brain growth." [HPO:curators]
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 HP:0001387 Joint stiffness "Joint stiffness is a perceived sensation of tightness in a joint or joints when attempting to move them after a period of inactivity. Joint stiffness typically subsides over time." [HPO:curators]
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 HP:0001508 Failure to thrive 
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 HP:0001518 Low birth weight 
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 HP:0001557 Prenatal movement abnormality 
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 HP:0001561 Polyhydramnios 
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 HP:0001562 Oligohydramnios 
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 HP:0001611 Nasal speech 
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 HP:0001623 breech presentation 
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 HP:0001762 Talipes equinovarus "Also called clubfoot typically has 4 main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg. Clubfoot is a complex, multifactorial deformity with genetic and intrauterine factors. One popular theory postulates that a clubfoot is a result of intrauterine maldevelopment of the talus that leads to adduction and plantarflexion of the foot. On radiographic projection a clubfoot can be noted as parallel axes of talus and calcaneus." [HPO:curators]
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 HP:0001838 Vertical talus 
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 HP:0001840 Metatarsus varus "Metatarsus varus (adductus) is one of the most common foot deformities, that is defined as a transverse plane deformity in Lisfranc s (tarsometatarsal) joints in which the metatarsals are deviated medially. The relationship between talus and calcaneus is normal. On inspection the toes angle abruptly towards the midline, creating a C-shaped lateral foot border with a prominent styloid process of the 5th metatarsal. The result is that the forefoot is twisted inwards relative to the heel, so that the sole faces the midline." [HPO:curators]
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 HP:0001848 Calcaneovalgus deformities 
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 HP:0001883 Talipes 
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 HP:0001945 Fever 
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 HP:0002047 Malignant hyperthermia "Malignant hyperthermia is characterized by a rapid increase in temperature to 39-42 degrees C in response to inhalational anesthetics such as halothane or to muscle relaxants such as succinylcholine." [HPO:curators]
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 HP:0002167 Neurological speech impairment 
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 HP:0002365 Hypoplasia of the brainstem 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002751 Kyphoscoliosis 
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 HP:0002804 Arthrogryposis multiplex congenita 
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 HP:0002827 Dislocated hips 
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 HP:0002937 Hemivertebrae 
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 HP:0002948 Vertebral fusion "A developmental defect leading to the union of two adjacent vertebrae." [HPO:curators]
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 HP:0002987 Elbow contractures 
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 HP:0003044 Shoulder contractures 
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 HP:0003049 Ulnar deviation of the wrist 
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 HP:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
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 HP:0003272 Abnormality of the hip "An abnormality of the hip joint or the surrounding anatomic region." [HPO:curators]
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 HP:0003273 Hip contractures 
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 HP:0003298 Spina bifida occulta "The closed form of spina bifida." [HPO:curators]
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 HP:0003302 Spondylolisthesis 
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 HP:0003422 Vertebral segmentation defects 
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0005272 Prominent nasolabial folds 
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 HP:0005684 Distal arthrogryposis 
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 HP:0005830 Partial flexion contractures of fingers and toes 
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 HP:0006109 Aplasia of the interphalangeal creases "Absence of the interphalangeal creases of the fingers." [HPO:curators]
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 HP:0006380 Knee flexion deformities 
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 HP:0006501 Aplasia/Hypoplasia of the radius "A small/hypoplastic or absent/aplastic radius." [HPO:curators]
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 HP:0006958 Abnormal auditory evoked potentials "An abnormality of the auditory evoked potentials, which are used to trace the signal generated by a sound, from the cochlear nerve, through the lateral lemniscus, to the medial geniculate nucleus, and to the cortex." [HPO:curators]
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 HP:0007598 Bilateral single palmar creases 
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 HP:0008368 Synostosis involving tarsal bones 
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 HP:0008872 Feeding problems in infancy 
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 HP:0008897 Growth retardation, progressive 
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 HP:0009465 Ulnar deviation of fingers 
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 HP:0009473 Joint contractures involving the joints of the hand 
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 HP:0010489 Aplasia of the palmar creases "Absence of the palmar creases." [HPO:curators]
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 HP:0010557 Overlapping fingers "Overlapping of the fingers occuring as the result of a deviation of the fingers from their normal position." [HPO:curators]
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 HP:0010751 Chin dimple "A persistent midline depression of the skin over the fat pad of the chin." [pmid:19125436]
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 HP:0011220 Prominent forehead "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436]
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 HP:0011824 Chin with H-shaped crease "H-shaped crease in the fat pad of the chin." [pmid:19125436]
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 HP:0012368 Flat face "Absence of concavity or convexity of the face when viewed in profile." [pmid:19125436]
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 HP:0012385 Camptodactyly "The distal interphalangeal joint and/or the proximal interphalangeal joint of the fingers or toes cannot be extended to 180 degrees by either active or passive extension." [HPO:probinson]
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 HP:0100490 Camptodactyly (hands) "Contractures of one ore more joints of the fingers." [HPO:sdoelken]
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 HP:0100790 Hernia 
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 HP:0100830 Round ear 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000134571 MYBPC3 / Q14896 / myosin binding protein C, cardiac  / complex / reaction
 ENSG00000155657 TTN / titin / Q8WZ42  / complex / reaction
 ENSG00000086967 MYBPC2 / Q14324 / myosin binding protein C, fast type  / complex / reaction
 ENSG00000196091 MYBPC1 / Q00872 / myosin binding protein C, slow type  / complex / reaction
 ENSG00000197616 MYH6 / P13533 / myosin heavy chain 6  / reaction / complex
 ENSG00000133020 MYH8 / P13535 / myosin heavy chain 8  / reaction / complex
 ENSG00000160808 MYL3 / P08590 / myosin light chain 3  / complex / reaction
 ENSG00000109063 MYH3 / P11055 / myosin heavy chain 3  / reaction / complex
 ENSG00000198336 MYL4 / P12829 / myosin light chain 4  / reaction / complex
 ENSG00000111245 MYL2 / P10916 / myosin light chain 2  / complex / reaction
 ENSG00000168530 MYL1 / P05976 / myosin light chain 1  / reaction / complex






 

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