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MED27

mediator complex subunit 27

HCNC Approved Symbol
MED27 (HGNC:2377)
Genomic Coordinates
9:131,860,112 - 132,079,867 (9q34.13)
Synonyms
TRAP37, CRSP34, MED3, CRSP8
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia
619286AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MED27 gene.

Frequently observed phenotypes

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

No Results