TTTY22
Chr Ytestis expressed transcript, Y-linked 22
Also known as: NCRNA00147
I cannot provide a clinical summary for TTTY22 as no functional or clinical information has been provided in the data below the gene name. This gene appears to be from the Y chromosome based on the "TTTY" prefix, but without specific information about protein function, associated diseases, or inheritance patterns, I cannot generate an accurate clinical summary following the guidelines.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
57 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 | — | — | — | — | 50 |
Likely Pathogenic | — | — | — | — | 2 |
VUS | — | — | — | — | 4 |
Likely Benign | — | — | — | — | 1 |
Benign | — | — | — | — | 0 |
| Total | — | 57 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
TTTY22 · 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