Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 53904
MIM: 606808
HGNC: 7601
Ensembl: ENSG00000095777
Variants:
dbSNP: 53904
ClinVar: 53904
TCGA: ENSG00000095777
COSMIC: MYO3A
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38042485 | 2024 | The dynamics of actin protrusions can be controlled by tip-localized myosin motors. | 0 |
| 38042485 | 2024 | The dynamics of actin protrusions can be controlled by tip-localized myosin motors. | 0 |
| 33953343 | 2022 | Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss. | 3 |
| 34423747 | 2022 | Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment. | 0 |
| 34788109 | 2022 | Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism. | 1 |
| 33953343 | 2022 | Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss. | 3 |
| 34423747 | 2022 | Molecular insights into MYO3A kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairment. | 0 |
| 34788109 | 2022 | Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism. | 1 |
| 33078831 | 2021 | Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon. | 7 |
| 33078831 | 2021 | Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon. | 7 |
| 32519820 | 2020 | A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family. | 5 |
| 32519820 | 2020 | A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family. | 5 |
| 29880844 | 2018 | Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. | 12 |
| 29880844 | 2018 | Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. | 12 |
| 26785147 | 2016 | Myosin III-mediated cross-linking and stimulation of actin bundling activity of Espin. | 15 |
Citation
Dessen P
MYO3A (myosin IIIA)
Atlas Genet Cytogenet Oncol Haematol. 2006-10-01
Online version: http://atlasgeneticsoncology.org/gene/43366/myo3a
