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FLASH GENE
Symbol IFNB1 contributors: mct - updated : 26-03-2020
HGNC name interferon, beta 1, fibroblast
HGNC id 5434
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein 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
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
SystemTypeDisorderPubmed
immunologyautoimmunemultiple sclerosis
major disease-modifying agent used for the treatment of multiple sclerosis (MS)
ANIMAL & CELL MODELS
  • 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