Variant "STIP1:c.151-1291A>C"
Search result: 1 record
Variant information
Gene:
Variant:
STIP1:c.151-1291A>C 
Genomic location:
chr11:63959259(hg19) 
HGVS:
SO Term RefSeq
protein_coding NM_001282652.1:c.151-1291A>C
protein_coding NM_001282653.1:c.10-1291A>C
protein_coding NM_006819.2:c.10-1291A>C
dbSNP ID:
GWAS trait:
no data 
Modifier statisitcs
Record:
Disorder:
Reference:
Effect type:
Expressivity(1)  
Modifier effect:
Altered response to corticosteroid(1)  
Detail:
  • Target disease:
    Asthma (DOID_2841)
    Effect type:
    Expressivity 
    Modifier effect:
    Altered response to corticosteroid 
    Evidence:
    From review article 
    Effect:
    Mutations in STIP1 is Associated with corticosteroid response
    Reference:
    Title:
    Genetic basis for personalized medicine in asthma.
    Species studied:
    Human
    Abstract:
    There is heterogeneity in patient responses to current asthma medications. Significant progress has been made identifying genetic polymorphisms that influence the efficacy and potential for adverse effects to asthma drugs, including; β(2)-adrenergic receptor agonists, corticosteroids and leukotriene modifiers. Pharmacogenetics holds great promise to maximise clinical outcomes and minimize adverse effects. Asthma is heterogeneous with respect to clinical presentation and inflammatory mechanisms underlying the disease, which is likely to contribute to variable results in clinical trials targeting specific inflammatory mediators. Genome-wide association studies have begun to identify genes underlying asthma (e.g., IL1RL1), which represent future therapeutic targets. In this article, we review and update the pharmacogenetics of current asthma therapies and discuss the genetics underlying selected Phase II and future targets.