The PTS gene is associated with autosomal recessive tetrahydrobiopterin-deficient hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency (MedGen UID: 209234).
Order this gene as a single gene test.
Invitae tests that include this gene:
An estimated 1-3% of hyperphenylalaninemia cases are due to defects in tetrahydrobiopterin metabolism. Of the 1-3% of cases, approximately 60% of them are due to 6-pyruvoyltetrahydropterin synthase (PTS) deficiency (PMID: 19234759).
The PTS gene encodes the enzyme, 6-pyruvoyltetrahydropterin synthase, which is involved in the second of three steps in the de novo biosynthesis of tetrahydrobiopterin (BH4). In the second step, 6-pyruvoyltetrahydropterin synthase removes triphospate from 7,8-dihydroneopterin triphosphate to create 6-pyruvoyl tetrahydropterin in a two step reaction (PMID: 19234759).
Invitae is a College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified clinical diagnostic laboratory performing full-gene sequencing and deletion/duplication analysis using next-generation sequencing technology (NGS).
Our sequence analysis covers clinically important regions of each gene, including coding exons, +/- 10 base pairs of adjacent intronic sequence in the transcript listed below. In addition, analysis covers the select non-coding variants specifically defined in the table below. Any variants that fall outside these regions are not analyzed. Any specific limitations in the analysis of these genes are also listed in the table below.
Our analysis detects most intragenic deletions and duplications at single exon resolution. However, in rare situations, single-exon copy number events may not be analyzed due to inherent sequence properties or isolated reduction in data quality. If you are requesting the detection of a specific single-exon copy number variation, please contact Client Services before placing your order.
|Gene||Transcript reference||Sequencing analysis||Deletion/Duplication analysis|