FAM199X
Chr Xfamily with sequence similarity 199, X-linked
Also known as: CXorf39
I don't have sufficient information about the FAM199X gene to write a clinical summary. The gene name suggests it's located on the X chromosome, but I would need specific data about the protein function, associated diseases, and clinical phenotypes to provide an accurate summary according to your guidelines.
Population Genetics & Constraint
gnomAD v4 — loss-of-function & missense intolerance
More LoF-intolerant than ~75% of genes
Moderately missense-constrained (top ~2.5%)
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
FAM199X · 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