Mason-Type Diabetes Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A genetic disease that has_material_basis_in mutations in the MODY genes disrupting insulin production. (Human Disease Ontology, DOID_0050524)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C562772
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Genes

2 genes/proteins associated with the disease Mason-Type Diabetes from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HNF4A hepatocyte nuclear factor 4, alpha 2.88009
GCK glucokinase (hexokinase 4) 2.88009