Gene entry
FTCD
formimidoyltransferase cyclodeaminase
- Chromosome
- 21
- Cytoband
- 21q22.3
- Variants (rsID)
- 16
FTCD is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.3). Its official name is “formimidoyltransferase cyclodeaminase”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs116089237Benignsingle nucleotide variantGlutamate formiminotransferase deficiency
- rs61735836Benignsingle nucleotide variantGlutamate formiminotransferase deficiency
- rs149266909Conflicting interpretationssingle nucleotide variantGlutamate formiminotransferase deficiency
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.