TTTY17A
Chr Ytestis expressed transcript, Y-linked 17A
Also known as: NCRNA00140, TTTY17
Based on the provided information, I cannot write a clinical gene summary for TTTY17A. The RefSeq description only indicates this is one of three copies of a gene located on chromosome Y, but provides no information about protein function, associated diseases, or clinical phenotypes. Additional clinical and functional data would be needed to create an informative summary for a pediatric neurogenetics portal.
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 | — | — | — | — | 76 |
Likely Pathogenic | — | — | — | — | 4 |
VUS | — | — | — | — | 14 |
Likely Benign | — | — | — | — | 10 |
Benign | — | — | — | — | 1 |
| Total | — | 105 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
TTTY17A · 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