Symbol
| IFNB1
| contributors: mct - updated : 26-03-2020
|
HGNC name
| interferon, beta 1, fibroblast
|
HGNC id
| 5434
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --over
|  
|
in dermatomyositis and polymyositis | constitutional
|  
|  
| --low
|  
|
most lung cells from stable Chronic Obstructive Pulmonary Disease (COPD) patients show a constitutive decreased expression of IFNB1, IRF7, DDX58 and IFIH1, suggesting that this deficiency is the main cause of their acute viral exacerbations | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
|
System | Type | Disorder | Pubmed |
immunology | autoimmune | multiple sclerosis | |
major disease-modifying agent used for the treatment of multiple sclerosis (MS) |
| | | |
| overexpression of Ifnb1 in the CNS of adult wild-type mice, but not of mice lacking IFN-I receptor on their microglia, induces an ageing-like transcriptional microglial signature, and impairs cognitive performance | |
Ifnb mutant mice is a model for sporadic Lewy body and Parkinson's disease dementia |