Gene entry

ATP6AP2

ATPase H+ transporting accessory protein 2

Chromosome: X
Cytoband: Xp11.4
Variants (rsID): 6

ATP6AP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.4). Its official name is “ATPase H+ transporting accessory protein 2”. The reference table lists 6 variants (rsID) for this gene.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Clinically classified variants

1 reference-table entries with clinical significance.

rs9014Benignsingle nucleotide variantSyndromic X-linked intellectual disability Hedera type|History of neurodevelopmental disorder

Other listed variants

rs6609080
rs67157095
rs113496360
rs142151739
rs368776566

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.