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MEGF10

multiple EGF like domains 10

HCNC Approved Symbol
MEGF10 (HGNC:29634)
Genomic Coordinates
5:127,229,300 - 127,461,222 (5q23.2)
Synonyms
KIAA1780, SR-F3
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Congenital myopathy 10A, severe variant
614399AR
Congenital myopathy 10B, mild variant
620249AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MEGF10 gene.

Frequently observed phenotypes

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

No Results