TTTY17C
Chr Ytestis expressed transcript, Y-linked 17C
Also known as: NCRNA00142
The protein function and clinical associations of TTTY17C are not well characterized. This gene is located on the Y chromosome and would follow Y-linked inheritance patterns, but no specific diseases or phenotypes have been definitively linked to mutations in this gene based on the available information.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
105 submitted variants in ClinVar
Classification Summary
Curated Variants Distribution
Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable
| Classification | LoF | Missense + Inframe | Non-coding | Synonymous | Total |
|---|---|---|---|---|---|
Pathogenic | — | — | — | — | 75 |
Likely Pathogenic | — | — | — | — | 3 |
VUS | — | — | — | — | 20 |
Likely Benign | — | — | — | — | 6 |
Benign | — | — | — | — | 1 |
| Total | — | 105 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
TTTY17C · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →No open access results found
External Resources
Links to major genomics databases and tools