USP9X Summary

This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

USP9X Details

Gene Symbol : USP9X

Gene Name : Ubiquitin specific peptidase 9, X-linked

Chromosome : CHR X: 410,854,19-412,365,78

Locus : Xp11.4

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ATP6AP2 Summary

This gene encodes a protein that is associated with adenosine triphosphatases (ATPases). Proton-translocating ATPases have fundamental roles in energy conservation, secondary active transport, acidification of intracellular compartments, and cellular pH homeostasis. There are three classes of ATPases- F, P, and V. The vacuolar (V-type) ATPases have a transmembrane proton-conducting sector and an extramembrane catalytic sector. The encoded protein has been found associated with the transmembrane sector of the V-type ATPases. [provided by RefSeq, Jul 2008]

ATP6AP2 Details

Gene Symbol : ATP6AP2

Gene Name : ATPase H+ transporting accessory protein 2

Chromosome : CHR X: 405,809,63-406,066,36

Locus : Xp11.4

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