med17 mediator complex subunit 17
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|Human (12 sources): Clonus, Diffuse cerebral atrophy, Dysphagia, Failure to thrive, Feeding difficulties, Global developmental delay, Hyperreflexia, Hypsarrhythmia, Progressive microcephaly, Secondary microcephaly, [+]|
|Mouse (2 sources): embryonic lethality prior to organogenesis, preweaning lethality, incomplete penetrance|
View all ortholog results at Monarch