The CTDP1 gene is associated with autosomal recessive congenital cataracts with facial dysmorphism and neuropathy (CCFDN) (Medgen UID: 346973).
Order this gene as a single gene test.
CTDP1: Analysis is limited to the NM_004715.4:c.863+389C>T variant.
Invitae tests that include this gene:
The CTDP1 gene encodes the carboxy-terminal domain phosphatase 1 protein. This protein regulates transcription by controlling the level of phosphorylation of the carboxy-terminal domain (CTD) of the POLR2A subunit of RNA polymerase II. The CTDP1 protein has also been implicated in recruitment of splicing machinery and chromatin remodeling (PMID: 9765293).
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, and select noncoding variants. Our assay provides a Q30 quality-adjusted mean coverage depth of 350x (50x minimum, or supplemented with additional analysis). Variants classified as pathogenic or likely pathogenic are confirmed with orthogonal methods, except individual variants that have high quality scores and previously validated in at least ten unrelated samples.
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|
*CTDP1: Analysis is limited to the NM_004715.4:c.863+389C>T variant.