Symbol
| NOBOX
| contributors: mct - updated : 23-01-2017
|
HGNC name
| NOBOX oogenesis homeobox
|
HGNC id
| 22448
|
corresponding disease(s)
|
POF5
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
| germinal mutation
|  
|  
|  
|
ovarian failure | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| abolishment of the transition from germ cell cysts to primordial follicles in the ovaries of Nobox deficient mice is caused by defects in germ cell cyst breakdown, leading to the formation of syncytial follicles instead of primordial follicles |