Symbol
| MYO18B
| contributors: mct - updated : 23-08-2014
|
HGNC name
| myosin XVIIIB
|
HGNC id
| 18150
|
corresponding disease(s)
|
KFS4
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
| somatic mutation
|  
|  
|  
|
in lung and ovarian carcinoma | tumoral
|  
|  
| --low
|  
|
by hypermethylation in ovarian cancer | tumoral
|  
|  
|  
| loss of function
|
in colorectal cancer | tumoral
|  
| LOH
|  
|  
|
in lung cancer | tumoral
|  
|  
| --low
|  
|
by promoter DNA methylation and histone deacetylation, was observed in 70p100 of lung cancers | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| deficiency of Myo18B caused an embryonic lethality in mice accompanied by disruption of myofibrillar structures in cardiac myocytes at embryonic day 10.5 |