Gene entry
TBX22
T-box transcription factor 22
- Chromosome
- X
- Cytoband
- Xq21.1
- Variants (rsID)
- 12
TBX22 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq21.1). Its official name is “T-box transcription factor 22”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs34244923Benignsingle nucleotide variantCleft palate with or without ankyloglossia, X-linked
- rs200060292Conflicting interpretationssingle nucleotide variantAbruzzo-Erickson syndrome|Cleft palate with or without ankyloglossia, X-linked
- rs199643713Likely benignsingle nucleotide variantCleft palate with or without ankyloglossia, X-linked
- rs104894943Pathogenicsingle nucleotide variantCleft palate with ankyloglossia
- rs104894944Pathogenicsingle nucleotide variantCleft palate with ankyloglossia
- rs104894945Pathogenicsingle nucleotide variantCleft palate with ankyloglossia
- rs104894946Pathogenicsingle nucleotide variantCleft palate with ankyloglossia
- rs28935177Pathogenicsingle nucleotide variantCleft palate with ankyloglossia
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.