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EPHA10

EPH receptor A10

HCNC Approved Symbol
EPHA10 (HGNC:19987)
Genomic Coordinates
1:37,713,880 - 37,765,120 (1p34.3)
Synonyms
FLJ16103, FLJ33655
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Deafness, autosomal dominant 88
620283AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the EPHA10 gene.

Frequently observed phenotypes

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

No Results