Gene entry
FAM111A
FAM111 trypsin like peptidase A
- Chromosome
- 11
- Cytoband
- 11q12.1
- Variants (rsID)
- 2
FAM111A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q12.1). Its official name is “FAM111 trypsin like peptidase A”. The reference table lists 2 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs587777011Pathogenicsingle nucleotide variantAutosomal dominant Kenny-Caffey syndrome|Osteocraniostenosis|Osteocraniostenosis|Autosomal dominant Kenny-Caffey syndrome|Inborn genetic diseases
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.