Xenbase is undergoing scheduled maintenance Wednesday, June 14 and Thursday, June 15, 2023. Xenbase will be unavailable on those days.

Click on this message to dismiss it.
Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (0) GO Terms (4) Nucleotides (126) Proteins (39) Interactants (33) Wiki
XB-GENEPAGE-1008313

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