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AFG2B

AFG2 AAA ATPase homolog B

HCNC Approved Symbol
AFG2B (HGNC:28762)
Genomic Coordinates
15:45,402,336 - 45,421,415 (15q21.1)
Synonyms
MGC5347, FLJ12286, SPATA5L1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Deafness, autosomal recessive 119
619615AR
Neurodevelopmental disorder with hearing loss and spasticity
619616AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the AFG2B gene.

Frequently observed phenotypes

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

No Results