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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.

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.