MYO18B (myosin XVIIIB)

2003-02-01  

Identity

HGNC
LOCATION
22q12.1
LOCUSID
ALIAS
KFS4
FUSION GENES

Other Information

Locus ID:

NCBI: 84700
MIM: 607295
HGNC: 18150
Ensembl: ENSG00000133454

Variants:

dbSNP: 84700
ClinVar: 84700
TCGA: ENSG00000133454
COSMIC: MYO18B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000133454ENST00000335473Q8IUG5
ENSG00000133454ENST00000407587Q8IUG5
ENSG00000133454ENST00000536101Q8IUG5
ENSG00000133454ENST00000539302F5H6I8
ENSG00000133454ENST00000540454A0A2Q2TCQ6
ENSG00000133454ENST00000543971H0YGQ4

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
331794332021Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism.0
335555052021Myosin18B predicts favorable prognosis of cutaneous squamous-cell carcinoma.2
331794332021Further delineation of MYO18B-related autosomal recessive Klippel-Feil syndrome with myopathy and facial dysmorphism.0
335555052021Myosin18B predicts favorable prognosis of cutaneous squamous-cell carcinoma.2
328776722020Myosin-18B Regulates Higher-Order Organization of the Cardiac Sarcomere through Thin Filament Cross-Linking and Thick Filament Dynamics.6
328776722020Myosin-18B Regulates Higher-Order Organization of the Cardiac Sarcomere through Thin Filament Cross-Linking and Thick Filament Dynamics.6
305810232019Myosin-18B Promotes the Assembly of Myosin II Stacks for Maturation of Contractile Actomyosin Bundles.20
305810232019Myosin-18B Promotes the Assembly of Myosin II Stacks for Maturation of Contractile Actomyosin Bundles.20
303906772018MYO18B promotes hepatocellular carcinoma progression by activating PI3K/AKT/mTOR signaling pathway.10
303906772018MYO18B promotes hepatocellular carcinoma progression by activating PI3K/AKT/mTOR signaling pathway.10
281047882017Myo18b is essential for sarcomere assembly in fast skeletal muscle.15
281047882017Myo18b is essential for sarcomere assembly in fast skeletal muscle.15
257484842015A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.29
257787782015Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.8
257484842015A 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/meetings/favicon/js/lib/all.min.js