Symbol
| PLXNA1
| contributors: mct - updated : 19-01-2022
|
HGNC name
| plexin A1
|
HGNC id
| 9099
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
| germinal mutation
|  
|  
|  
|
in developmental delay who developed parkinsonism | |
Susceptibility
|
to anosmic but also normosmic idiopathic hypogonadotropic hypogonadism (IHH) |
Variant & Polymorphism
other
| PLXNA1 variants cause not only anosmic but also normosmic IHH |
|
|
Candidate gene
Marker
Therapy target
| | | |