TTTY6B
Chr Ytestis expressed transcript, Y-linked 6B
The protein function and clinical significance of TTTY6B are not well established based on the available data. This gene is located on the Y chromosome and would follow patrilineal inheritance patterns, but no associated diseases or phenotypes have been definitively characterized. Further research is needed to determine its clinical relevance in pediatric neurology.
Some data sources returned errors (1)
ncbi: Error: NCBI fetch failed: 429 https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
99 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 | — | — | — | — | 73 |
Likely Pathogenic | — | — | — | — | 3 |
VUS | — | — | — | — | 13 |
Likely Benign | — | — | — | — | 8 |
Benign | — | — | — | — | 2 |
| Total | — | 99 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
TTTY6B · 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