| 摘要 |
PROBLEM TO BE SOLVED: To provide a method for diagnosis relating to one nucleotide polymorphism in human prostaglandin E2 receptor 1 (EP1-R) gene and the new corresponding allelic polypeptide encoded thereby. SOLUTION: This method for diagnosing the polymorphism in human EP1-R gene comprises the steps of determining the sequence(s) of a specific site or more in human EP1-R gene or 126th or 154th amino acid in EP1-R protein, and determining the state of human whose polymorphism in EP1-R gene was referred. |
