Symbol
| COMMD9
| contributors: mct - updated : 14-04-2021
|
HGNC name
| COMM domain containing 9
|
HGNC id
| 25014
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
|  
|  
| gain of function
|
in several non-small cell lung cancer (NSCLC) cell lines | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| Commd9 deletion in mice leads to embryonic lethality and complex cardiovascular alterations that bear hallmarks of Notch deficiency |