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AFG2A

AFG2 AAA ATPase homolog A

HCNC Approved Symbol
AFG2A (HGNC:18119)
Genomic Coordinates
4:122,923,078 - 123,319,433 (4q28.1)
Synonyms
SPAF, AFG2, SPATA5
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities
616577AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the AFG2A gene.

Frequently observed phenotypes

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

No Results