MYH10: Myosin Heavy Chain 10 - A Key Cytoskeletal Motor Protein

Comprehensive genomic, transcriptomic, and proteomic analysis of MYH10, including expression, mutations, and disease associations.

Gene Information Card

Symbol MYH10
Full Name Myosin Heavy Chain 10
Gene Type Protein coding
Chromosomal Location 17p13.1
NCBI Gene ID 4628 ncbi.nlm.nih.gov/gene/4628
Ensembl ID ENSG00000133026
UniProt ID P35580
OMIM ID 160776
HGNC ID 7568
Aliases NMHC IIB, NMMHC IIB, MGC134872

Description

MYH10 encodes the heavy chain of non-muscle myosin IIB, a member of the myosin superfamily. This protein is a major component of the cytoskeleton, involved in cell motility, adhesion, cytokinesis, and tissue morphogenesis. It functions as an actin-based motor ATPase, generating contractile force. Mutations and altered expression of MYH10 are associated with various cancers, developmental disorders, and cardiovascular diseases.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hereditary nonpolyposis colorectal cancer (Lynch syndrome) MYH10 interacts with mismatch repair proteins; loss of expression may contribute to microsatellite instability. ClinVar, COSMIC
Breast cancer Overexpression of MYH10 correlates with poor prognosis; promotes cell migration and invasion. COSMIC, NCBI PubMed
Cardiomyopathy, dilated MYH10 variants disrupt sarcomere organization and contractile function. OMIM, ClinVar
Developmental brain malformations MYH10 mutations impair neuronal migration and cortical development. OMIM, ClinVar

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 18.5 High
Heart 15.2 High
Lung 12.8 Medium
Liver 8.1 Medium
Kidney 10.3 Medium
Skeletal muscle 6.7 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 22.4 Cervical cancer cell line; high expression
MCF7 18.9 Breast cancer cell line; moderate expression
A549 15.6 Lung cancer cell line; moderate expression
HEK293 12.3 Embryonic kidney; moderate expression
K562 9.8 Leukemia cell line; low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.4537C>T (p.Arg1513Trp) Missense <0.01% Altered ATPase activity; associated with dilated cardiomyopathy
c.2101G>A (p.Glu701Lys) Missense <0.01% Impaired actin binding; linked to developmental brain malformations
c.1234_1235insA (p.Thr412Asnfs*5) Frameshift <0.01% Loss of function; observed in colorectal cancer
c.2890A>G (p.Thr964Ala) Missense <0.01% Unknown significance; reported in COSMIC
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations leading to truncated protein or nonsense-mediated decay; associated with cancer and developmental defects.

Gain of Function (GOF)

Missense mutations that enhance ATPase activity or actin binding, potentially promoting cell migration in cancer.

Dominant Negative (DN)

Missense mutations that disrupt filament assembly or motor function, interfering with wild-type myosin IIB activity.

Pathways

REACT:21333 - Smooth muscle contraction
REACT:21334 - Non-muscle myosin II signaling
REACT:21335 - Actin cytoskeleton regulation
REACT:21336 - Cell migration and adhesion

Protein Summary

Myosin heavy chain 10 (MYH10) is a 1960-amino acid protein that forms the heavy chain of non-muscle myosin IIB. It contains an N-terminal motor domain with ATPase activity, a neck region with IQ motifs for light chain binding, and a C-terminal tail domain involved in filament assembly. The protein is ubiquitously expressed, with highest levels in brain and heart. It plays critical roles in cytokinesis, cell polarity, and tissue integrity. Post-translational modifications include phosphorylation of the regulatory light chain, which controls its activity.

Related Products

Product name Cat.No. Species Gene ID
MYH10 Knockout HEK293 Cell Line EDJ-KQ2734 Human 4628 Details Get a Quote
MYH10 Knockout HeLa Cell Line EDJ-KQ22231 Human 4628 Details Get a Quote
MYH10 Knockout A-549 Cell Line EDJ-KQ23601 Human 4628 Details Get a Quote
MYH10 Knockout HCT 116 Cell Line EDJ-KQ23602 Human 4628 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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