Gene entry
ATP11C
ATPase phospholipid transporting 11C (ATP11C blood group)
- Chromosome
- X
- Cytoband
- Xq27.1
- Variants (rsID)
- 13
ATP11C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq27.1). Its official name is “ATPase phospholipid transporting 11C (ATP11C blood group)”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs2491014Not classifiedmissense_variant
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.
