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ATP11A

ATPase phospholipid transporting 11A

HCNC Approved Symbol
ATP11A (HGNC:13552)
Genomic Coordinates
13:112,690,038 - 112,887,168 (13q34)
Synonyms
ATPIH, ATPIS, KIAA1021
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Auditory neuropathy, autosomal dominant 2
620384AD
?Leukodystrophy, hypomyelinating, 24
619851AD
Deafness, autosomal dominant 84
619810AD

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the ATP11A gene.

Frequently observed phenotypes

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

No Results