Symbol
| RNF220
| contributors: mct - updated : 13-01-2022
|
HGNC name
| ring finger protein 220
|
HGNC id
| 25552
|
corresponding disease(s)
|
HLD23
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
| germinal mutation
|  
|  
|  
|
leads to male infertility with small-headed sperm | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| Rnf220-null mice show widespread alterations of ventral progenitor domains, including the loss of the p2 domain that produces V2 interneurons |