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VMA21 protein, human MeSH Supplementary Concept Data 2025


MeSH Supplementary
VMA21 protein, human
Unique ID
C540401
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C540401
Registry Numbers
EC 3.6.1.-
Heading Mapped to
*Vacuolar Proton-Translocating ATPases
Frequency
31
Note
mutations in this protein are associated with X-linked myopathy with excessive autophagy; GenBank AL833596
Source
Cell 2009 Apr 17;137(2):235-46
Date of Entry
2009/05/06
Revision Date
1955/01/01
VMA21 protein, human Preferred
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