DNA encoding human asthma associated factor 1
US6037149A · kind A · utility
5Cited by
10References
23Claims
0Family size
Assignee
Inventors
Key dates
| Filing date | Aug 23, 1996 |
| Grant date | Mar 14, 2000 |
| Priority date | — |
| Expiry date | Aug 23, 2016 |
Classification
- Technology area (CPC A)Human Necessities
- CPC primaryA61K38/00
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
A C to T DNA variation at position 3365 in exon 5 of the human Asthma Associated Factor 1 (AAF1) produces the predicted amino acid substitution of a methionine for a threonine at codon 117 of AAF1. When this substitution occurs in both alleles in one individual, it is associated with less evidence of atopic allergy including asthma, fewer abnormal skin test responses, and a lower serum total IgE. Thus, applicant has identified the existence of a non-asthmatic, non-atopic phenotype characterized by methionine at codon 117 when it occurs in both AAF1 gene products in one individual.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.