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ATP5MK

ATP synthase membrane subunit k

HCNC Approved Symbol
ATP5MK (HGNC:30889)
Genomic Coordinates
10:103,389,050 - 103,396,475 (10q24.33)
Synonyms
MGC14697, bA792D24.4, DAPIT, AGP, USMG5, ATP5MD
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Mitochondrial complex V (ATP synthase) deficiency, nuclear type 6
618683AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the ATP5MK gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results