External Ids for MIDN Gene
Previous GeneCards Identifiers for MIDN Gene
GeneCards Summary for MIDN Gene
MIDN (Midnolin) is a Protein Coding gene. Diseases associated with MIDN include Polyneuropathy Due To Drug and Inflammatory And Toxic Neuropathy. Gene Ontology (GO) annotations related to this gene include kinase binding.
UniProtKB/Swiss-Prot Summary for MIDN Gene
Facilitates ubiquitin-independent proteasomal degradation of polycomb protein CBX4. Plays a role in inhibiting the activity of glucokinase GCK and both glucose-induced and basal insulin secretion.