HMSNP; SPG57; TF6; TRKT3
The TFG gene is associated with autosomal dominant hereditary motor and sensory neuropathy, Okinawa type (HMSNO) (MedGen UID: 346886). Additionally, the TFG gene has preliminary evidence supporting a correlation with autosomal dominant Charcot-Marie-Tooth disease, type 2 (CMT2) (PMID: 25098539) and autosomal recessive hereditary spastic paraplegia 57 (SPG57) (MedGen UID: 811490; PMID: 23479643).
Order this gene as a single gene test.
Invitae tests that include this gene:
The TFG gene encodes the TRK-fused gene protein. This gene is expressed in the nervous system where its protein product plays a role in the dynamic structuring of the endoplasmic reticulum.
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|