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MYH3 myosin heavy chain 3 [ Homo sapiens (human) ]

Gene ID: 4621, updated on 10-Mar-2024

Summary

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Official Symbol
MYH3provided by HGNC
Official Full Name
myosin heavy chain 3provided by HGNC
Primary source
HGNC:HGNC:7573
See related
Ensembl:ENSG00000109063 MIM:160720; AllianceGenome:HGNC:7573
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
DA8; DA2A; DA2B; DA2B3; HEMHC; SMHCE; MYHSE1; CPSFS1A; CPSFS1B; CPSKF1A; CPSKF1B; MYHC-EMB
Summary
Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008]
Expression
Biased expression in prostate (RPKM 18.9), esophagus (RPKM 4.8) and 5 other tissues See more
Orthologs
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Genomic context

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See MYH3 in Genome Data Viewer
Location:
17p13.1
Exon count:
43
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (10628532..10678417, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (10536104..10585897, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (10531849..10560626, complement)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene myosin heavy chain gene cluster antisense RNA Neighboring gene MED14-independent group 3 enhancer GRCh37_chr17:10395090-10396289 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr17:10399610-10400809 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr17:10407979-10409178 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr17:10427829-10429028 Neighboring gene myosin heavy chain 1 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr17:10446256-10447455 Neighboring gene myosin heavy chain 2 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:10475093-10475685 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:10520795-10521295 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:10521298-10521798 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:10521799-10522299 Neighboring gene uncharacterized LOC124903927 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11731 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 11732 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:10599827-10600650 Neighboring gene H3K27ac hESC enhancer GRCh37_chr17:10600651-10601475 Neighboring gene synthesis of cytochrome C oxidase 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr17:10616259-10616459 Neighboring gene ADP-ribose/CDP-alcohol diphosphatase, manganese dependent Neighboring gene transmembrane protein 220 Neighboring gene mago homolog 2, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. Recessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome. Hakonen AH, et al. Am J Med Genet A, 2020 Nov. PMID 32902138
  2. Identification of a novel pathogenic variant in the MYH3 gene in a five-generation family with CPSFS1A (Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1A). Zhang J, et al. Mol Genet Genomic Med, 2020 Oct. PMID 32767732, Free PMC Article
  3. Mutations in the tail domain of MYH3 contributes to atrial septal defect. Maran S, et al. PLoS One, 2020. PMID 32315303, Free PMC Article
  4. Identification of a novel pathogenic mutation of the MYH3 gene in a family with distal arthrogryposis type 2B. Wang WB, et al. Mol Med Rep, 2020 Jan. PMID 31746383
  5. [Analysis of MYH3 gene variation and prenatal diagnosis for two pedigrees affected with congenital arthrogryposis]. Xu X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2019 May 10. PMID 31030430

See all (52) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).
    Title: Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B).
  2. METTL3 achieves lipopolysaccharide-induced myocardial injury via m[6]A-dependent stabilization of Myh3 mRNA.
    Title: METTL3 achieves lipopolysaccharide-induced myocardial injury via m(6)A-dependent stabilization of Myh3 mRNA.
  3. Recessive MYH3 variants cause ""Contractures, pterygia, and variable skeletal fusions syndrome 1B"" mimicking Escobar variant multiple pterygium syndrome.
    Title: Recessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome.
  4. Identification of a novel pathogenic variant in the MYH3 gene in a five-generation family with CPSFS1A (Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1A).
    Title: Identification of a novel pathogenic variant in the MYH3 gene in a five-generation family with CPSFS1A (Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1A).
  5. Identification of a novel pathogenic mutation of the MYH3 gene in a family with distal arthrogryposis type 2B.
    Title: Identification of a novel pathogenic mutation of the MYH3 gene in a family with distal arthrogryposis type 2B.
  6. Report a case-control study investigating the role of MYH3 among non-syndromic atrial septal defect patients in contributing to septal development. The non-synonymous c. 3574G>A (p.Ala1192Thr) [p = 0.001, OR = 2.30 (1.36-3.87)] located within the tail domain indicated a highly conserved protein region.
    Title: Mutations in the tail domain of MYH3 contributes to atrial septal defect.
  7. two heterozygous variations of the MYH3 gene probably underlie the disease in the pedigrees
    Title: [Analysis of MYH3 gene variation and prenatal diagnosis for two pedigrees affected with congenital arthrogryposis].
  8. Our findings also support a role for MYH3 in both muscle and bone development, suggesting a phenotypic continuum in MYH3-related disorders.
    Title: A novel pathogenic MYH3 mutation in a child with Sheldon-Hall syndrome and vertebral fusions.
  9. Although some MYH3 variants cause dominant Spondylocarpotarsal synostosis syndrome, these data indicate that others (notably truncating variants) do not, except in the context of compound heterozygosity for a second hypomorphic allele.
    Title: Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.
  10. A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination.
    Title: A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination.
Submit: New GeneRIF Correction See all GeneRIFs (25)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description Tests
Arthrogryposis, distal, type 2B3
MedGen: C5193098 OMIM: 618436 GeneReviews: Not available
Compare labs
Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A
MedGen: C1867440 OMIM: 178110 GeneReviews: Not available
Compare labs
Contractures, pterygia, and variable skeletal fusions syndrome 1B
MedGen: C5193114 OMIM: 618469 GeneReviews: Not available
Compare labs
Freeman-Sheldon syndrome
MedGen: C0265224 OMIM: 193700 GeneReviews: Not available
Compare labs

EBI GWAS Catalog

Description
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
EBI GWAS Catalog

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables ATP binding IEA
Inferred from Electronic Annotation
more info
  
enables ATP hydrolysis activity IMP
Inferred from Mutant Phenotype
more info
 PubMed 
enables actin filament binding IBA
Inferred from Biological aspect of Ancestor
more info
  
enables actin filament binding IMP
Inferred from Mutant Phenotype
more info
 PubMed 
enables calmodulin binding NAS
Non-traceable Author Statement
more info
 PubMed 
enables microfilament motor activity IBA
Inferred from Biological aspect of Ancestor
more info
  
enables microfilament motor activity IMP
Inferred from Mutant Phenotype
more info
 PubMed 
enables microfilament motor activity NAS
Non-traceable Author Statement
more info
 PubMed 
enables myosin phosphatase activity TAS
Traceable Author Statement
more info
  
Process Evidence Code Pubs
involved_in ATP metabolic process IMP
Inferred from Mutant Phenotype
more info
 PubMed 
involved_in actin filament-based movement NAS
Non-traceable Author Statement
more info
 PubMed 
involved_in embryonic limb morphogenesis IC
Inferred by Curator
more info
 PubMed 
involved_in face morphogenesis IC
Inferred by Curator
more info
 PubMed 
involved_in muscle contraction IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in muscle filament sliding TAS
Traceable Author Statement
more info
  
involved_in muscle organ development TAS
Traceable Author Statement
more info
 PubMed 
involved_in sarcomere organization NAS
Non-traceable Author Statement
more info
 PubMed 
involved_in skeletal muscle contraction IMP
Inferred from Mutant Phenotype
more info
 PubMed 
Component Evidence Code Pubs
is_active_in cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in cytosol TAS
Traceable Author Statement
more info
  
located_in extracellular exosome HDA PubMed 
part_of muscle myosin complex NAS
Non-traceable Author Statement
more info
 PubMed 
part_of myosin II complex IBA
Inferred from Biological aspect of Ancestor
more info
  
is_active_in myosin filament IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in sarcomere NAS
Non-traceable Author Statement
more info
 PubMed 

General protein information

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Preferred Names
myosin-3
Names
myosin heavy chain, fast skeletal muscle, embryonic
myosin, heavy chain 3, skeletal muscle, embryonic
myosin, heavy polypeptide 3, skeletal muscle, embryonic
myosin, skeletal, heavy chain, embryonic 1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_011537.1 RefSeqGene

    Range
    4990..33767
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_002470.4 → NP_002461.2  myosin-3

    See identical proteins and their annotated locations for NP_002461.2

    Status: REVIEWED

    Source sequence(s)
    AC002347, AY517555, BP232093, BP232269, BP233220, BP370003, BQ956249, BX500019, BY796597, CD614924, X13988
    Consensus CDS
    CCDS11157.1
    UniProtKB/Swiss-Prot
    P11055, Q15492
    Related
    ENSP00000464317.1, ENST00000583535.6
    Conserved Domains (9) summary
    cd14913
    Location:100 → 767
    MYSc_Myh3; class II myosin heavy chain 3, motor domain
    pfam00063
    Location:88 → 767
    Myosin_head; Myosin head (motor domain)
    pfam01576
    Location:847 → 1924
    Myosin_tail_1; Myosin tail
    pfam02736
    Location:36 → 73
    Myosin_N; Myosin N-terminal SH3-like domain
    pfam07851
    Location:1739 → 1850
    TMPIT; TMPIT-like protein
    cl00459
    Location:1296 → 1408
    MIT_CorA-like; metal ion transporter CorA-like divalent cation transporter superfamily
    cl03075
    Location:843 → 962
    GrpE; nucleotide exchange factor GrpE
    cl12013
    Location:956 → 1063
    BAR; The Bin/Amphiphysin/Rvs (BAR) domain, a dimerization module that binds membranes and detects membrane curvature
    cl19764
    Location:1373 → 1506
    COG6; Conserved oligomeric complex COG6

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    10628532..10678417 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_011523870.4 → XP_011522172.1  myosin-3 isoform X1

    See identical proteins and their annotated locations for XP_011522172.1

    UniProtKB/Swiss-Prot
    P11055, Q15492
    Conserved Domains (9) summary
    cd14913
    Location:100 → 767
    MYSc_Myh3; class II myosin heavy chain 3, motor domain
    pfam00063
    Location:88 → 767
    Myosin_head; Myosin head (motor domain)
    pfam01576
    Location:847 → 1924
    Myosin_tail_1; Myosin tail
    pfam02736
    Location:36 → 73
    Myosin_N; Myosin N-terminal SH3-like domain
    pfam07851
    Location:1739 → 1850
    TMPIT; TMPIT-like protein
    cl00459
    Location:1296 → 1408
    MIT_CorA-like; metal ion transporter CorA-like divalent cation transporter superfamily
    cl03075
    Location:843 → 962
    GrpE; nucleotide exchange factor GrpE
    cl12013
    Location:956 → 1063
    BAR; The Bin/Amphiphysin/Rvs (BAR) domain, a dimerization module that binds membranes and detects membrane curvature
    cl19764
    Location:1373 → 1506
    COG6; Conserved oligomeric complex COG6

  2. XM_047436127.1 → XP_047292083.1  myosin-3 isoform X1

    UniProtKB/Swiss-Prot
    P11055, Q15492

  3. XM_011523871.3 → XP_011522173.1  myosin-3 isoform X1

    See identical proteins and their annotated locations for XP_011522173.1

    UniProtKB/Swiss-Prot
    P11055, Q15492
    Conserved Domains (9) summary
    cd14913
    Location:100 → 767
    MYSc_Myh3; class II myosin heavy chain 3, motor domain
    pfam00063
    Location:88 → 767
    Myosin_head; Myosin head (motor domain)
    pfam01576
    Location:847 → 1924
    Myosin_tail_1; Myosin tail
    pfam02736
    Location:36 → 73
    Myosin_N; Myosin N-terminal SH3-like domain
    pfam07851
    Location:1739 → 1850
    TMPIT; TMPIT-like protein
    cl00459
    Location:1296 → 1408
    MIT_CorA-like; metal ion transporter CorA-like divalent cation transporter superfamily
    cl03075
    Location:843 → 962
    GrpE; nucleotide exchange factor GrpE
    cl12013
    Location:956 → 1063
    BAR; The Bin/Amphiphysin/Rvs (BAR) domain, a dimerization module that binds membranes and detects membrane curvature
    cl19764
    Location:1373 → 1506
    COG6; Conserved oligomeric complex COG6

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    10536104..10585897 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_054316234.1 → XP_054172209.1  myosin-3 isoform X1

  2. XM_054316235.1 → XP_054172210.1  myosin-3 isoform X1

Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
P11055.3 GenPept UniProtKB/Swiss-Prot:P11055

Gene LinkOut

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