TTTY11
Chr Ytestis expressed transcript, Y-linked 11
Also known as: NCRNA00134, TTY11
I cannot provide a clinical summary for TTTY11 as no information about its protein function, associated diseases, or inheritance pattern was provided in the data below the instructions. A clinical gene summary requires specific details about what the encoded protein does, what phenotypes result from mutations, and the mode of inheritance to be clinically useful for child neurologists.
Some data sources returned errors (1)
omim: Error: OMIM fetch failed: 429
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
66 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 | — | — | — | — | 52 |
Likely Pathogenic | — | — | — | — | 2 |
VUS | — | — | — | — | 6 |
Likely Benign | — | — | — | — | 5 |
Benign | — | — | — | — | 0 |
| Total | — | 65 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
TTTY11 · 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