Gene entry
AMELX
amelogenin X-linked
- Chromosome
- X
- Cytoband
- Xp22.2
- Variants (rsID)
- 10
AMELX is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.2). Its official name is “amelogenin X-linked”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs104894733Pathogenicsingle nucleotide variantAmelogenesis imperfecta type 1E
- rs104894734Pathogenicsingle nucleotide variantAmelogenesis imperfecta type 1E
- rs104894736Pathogenicsingle nucleotide variantAmelogenesis imperfecta type 1E
- rs104894737Pathogenicsingle nucleotide variantAmelogenesis imperfecta type 1E
- rs104894738Pathogenicsingle nucleotide variantAmelogenesis imperfecta type 1E
- rs387906488PathogenicDeletionAmelogenesis imperfecta type 1E
- rs387906489PathogenicDeletionAmelogenesis imperfecta type 1E
- rs387906490PathogenicDeletionAmelogenesis imperfecta type 1E
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.