Symbol
| GPHN
| contributors: mct/npt/pgu - updated : 09-11-2016
|
HGNC name
| gephyrin
|
HGNC id
| 15465
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
| fusion
|  
|  
|  
|
with MLL in t(11;14) (q23;q24) in acute monoblastic leukemia | constitutional
|  
|  
| --low
|  
|
significantly lower in the temporal neocortex of temporal lobe epilepsy patients compared to the controls | constitutional
|  
|  
| --low
|  
|
in Alzheimer Disease | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| Gephyrin-deficient (geph(-/-)) mice die after birth due to disinhibition of motor and sensory pathways resulting from a lack of postsynaptic glycine receptor and GABA(A) receptor clusters | |
|