SRXX1; SRXY1; TDF; TDY
The SRY gene is associated with 46,XY and 46,XX disorders of sex development (MedGen UID: 412662, 411324).
Order this gene as a single gene test.
Invitae tests that include this gene:
The SRY gene is the principal gene associated with 46,XX testicular DSD and accounts for approximately 80% of affected individuals (PMID: 20301589). Alterations of SRY are a rare cause of 46,XY Disorders of Sex Development but cause up to 15% of 46,XY complete gonadal dysgenesis (PMID: 1415266, 20301714).
The SRY gene encodes a transcription factor that is involved in the development of male reproductive organs, and suppression of female reproductive organ development (PMID: 19513096, 25246082).
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|