FAM225B
Chr 9family with sequence similarity 225 member B
Also known as: C9orf110, LINC00256B, NCRNA00256B
I cannot provide a clinical gene summary for FAM225B based on the information provided, as no data about the protein function, associated diseases, inheritance pattern, or clinical phenotypes has been included in your request. To write an accurate clinical summary following your guidelines, I would need specific information about what the FAM225B protein does, what conditions result from mutations in this gene, and the inheritance pattern of those conditions.
Population Genetics & Constraint
Constraint data not available from gnomAD.
ClinVar Variant Classifications
14 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 | — | — | — | — | 14 |
Likely Pathogenic | — | — | — | — | 0 |
VUS | — | — | — | — | 0 |
Likely Benign | — | — | — | — | 0 |
Benign | — | — | — | — | 0 |
| Total | — | 14 | |||
Counts from ClinVar esearch · Updated hourly
View in ClinVar →Protein Context — Lollipop Plot
FAM225B · 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 →External Resources
Links to major genomics databases and tools