Symbol
| NRGN
| contributors: mct - updated : 10-03-2020
|
HGNC name
| neurogranin (protein kinase C substrate, RC3)
|
HGNC id
| 8000
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --over
|  
|
in patients with structural lesions resulting from mild traumatic brain injuries | constitutional
|  
|  
| --over
|  
|
of GAP43 and neurogranin (NRGN) in CSF from ALzheimer disease patients | constitutional
|  
|  
| --over
|  
|
in the AD patients than in cognitively healthy controls | |
Susceptibility
|
to schizophrenia |
Variant & Polymorphism
SNP
, other
| polymorphism rs12807809 located upstream of the neurogranin (NRGN) gene has been identified as a risk variant for schizophrenia |
|
|
Candidate gene
| may have a role in neurocognitive and behavioral defects in the 11qter deletion disorder DEL11QD (Coldren 2009) |
Marker
| NRGN and NPTXR concentrations in CSF are promising synaptic dysfunction biomarkers reflecting pathological changes in AD |
Therapy target
| |