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EPS8L2

EPS8 signaling adaptor L2

HCNC Approved Symbol
EPS8L2 (HGNC:21296)
Genomic Coordinates
11:706,231 - 727,727 (11p15.5)
Synonyms
FLJ21935, FLJ22171, MGC3088
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the EPS8L2 gene.

Frequently observed phenotypes

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

Hearing loss
 1 (100.0%)
EPS8L2 - Gene browser | 3billion