HUPF3B; MRX62; MRXS14; RENT3B; UPF3BP1; UPF3BP2; UPF3BP3; UPF3X; Upf3p-X
The UPF3B gene currently has no well-established disease association; however, there is preliminary evidence supporting a correlation with X-linked intellectual disability (PMID: 19238151, 22957832), Lujan-Fryns syndrome (LFS) (PMID: 17704778, 19238151), and Opitz-Kaveggia syndrome (OKS) (PMID: 17704778).
Order this gene as a single gene test.
UPF3B: Deletion/duplication analysis is not offered for exons 2-3.
Invitae tests that include this gene:
The UPF3B gene encodes a protein that binds to and assists in the turnover of improper mRNA transcripts through the process of nonsense-mediated decay.
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|
*UPF3B: Deletion/duplication analysis is not offered for exons 2-3.