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FAM197Y10
Chr Yfamily with sequence similarity 197 Y-linked member 10
I cannot write a clinical summary for FAM197Y10 as no information about this gene's protein function, associated diseases, or inheritance pattern has been provided in the data below. To create an accurate clinical summary following the specified guidelines, I would need details about what the protein does, what conditions result from mutations in this gene, and the inheritance pattern.
Some data sources returned errors (1)
ensembl: Error: Ensembl fetch failed: 400 for https://rest.ensembl.org/lookup/symbol/homo_sapiens/FAM197Y10?content-type=application/json&expand=1
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
80 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 | — | — | — | — | 66 |
Likely Pathogenic | — | — | — | — | 1 |
VUS | — | — | — | — | 7 |
Likely Benign | — | — | — | — | 6 |
Benign | — | — | — | — | 0 |
| Total | — | 80 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
FAM197Y10 · 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 publications found for FAM197Y10
External Resources
Links to major genomics databases and tools