Symbol
| MEIOB
| contributors: mct - updated : 13-04-2021
|
HGNC name
| meiosis-specific with OB domain-containing protein
|
HGNC id
| 28569
|
corresponding disease(s)
|
SPGF22
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
| germinal mutation
|  
|  
|  
|
a truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 | |
Candidate gene
Marker
Therapy target
| | | |
| Meiob-null mouse mutants exhibit a failure in meiosis and sterility in both sexes |