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ATP6V1C2

ATPase H+ transporting V1 subunit C2

HCNC Approved Symbol
ATP6V1C2 (HGNC:18264)
Genomic Coordinates
2:10,720,943 - 10,785,110 (2p25.1)
Synonyms
VMA5, ATP6C2
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there is 1 patient* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

ATP6V1C2 - Gene browser | 3billion