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: 84700
MIM: 607295
HGNC: 18150
Ensembl: ENSG00000133454
Variants:
dbSNP: 84700
ClinVar: 84700
TCGA: ENSG00000133454
COSMIC: MYO18B
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33179433 | 2021 | Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism. | 0 |
| 33555505 | 2021 | Myosin18B predicts favorable prognosis of cutaneous squamous-cell carcinoma. | 2 |
| 33179433 | 2021 | Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism. | 0 |
| 33555505 | 2021 | Myosin18B predicts favorable prognosis of cutaneous squamous-cell carcinoma. | 2 |
| 32877672 | 2020 | Myosin-18B Regulates Higher-Order Organization of the Cardiac Sarcomere through Thin Filament Cross-Linking and Thick Filament Dynamics. | 6 |
| 32877672 | 2020 | Myosin-18B Regulates Higher-Order Organization of the Cardiac Sarcomere through Thin Filament Cross-Linking and Thick Filament Dynamics. | 6 |
| 30581023 | 2019 | Myosin-18B Promotes the Assembly of Myosin II Stacks for Maturation of Contractile Actomyosin Bundles. | 20 |
| 30581023 | 2019 | Myosin-18B Promotes the Assembly of Myosin II Stacks for Maturation of Contractile Actomyosin Bundles. | 20 |
| 30390677 | 2018 | MYO18B promotes hepatocellular carcinoma progression by activating PI3K/AKT/mTOR signaling pathway. | 10 |
| 30390677 | 2018 | MYO18B promotes hepatocellular carcinoma progression by activating PI3K/AKT/mTOR signaling pathway. | 10 |
| 28104788 | 2017 | Myo18b is essential for sarcomere assembly in fast skeletal muscle. | 15 |
| 28104788 | 2017 | Myo18b is essential for sarcomere assembly in fast skeletal muscle. | 15 |
| 25748484 | 2015 | A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B. | 29 |
| 25778778 | 2015 | Lack of replication for the myosin-18B association with mathematical ability in independent cohorts. | 8 |
| 25748484 | 2015 | A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B. | 29 |
Citation
Dessen P
MYO18B (myosin XVIIIB)
Atlas Genet Cytogenet Oncol Haematol. 2003-02-01
Online version: http://atlasgeneticsoncology.org/gene/41481/myo18b-(myosin-xviiib)
