Aliases for OMD Gene
Previous GeneCards Identifiers for OMD Gene
GeneCards Summary for OMD Gene
OMD (Osteomodulin) is a Protein Coding gene. Diseases associated with OMD include Occult Macular Dystrophy and Hallermann-Streiff Syndrome. Among its related pathways are Glycosaminoglycan metabolism and Defective B3GAT3 causes JDSSDHD. An important paralog of this gene is ECM2.
UniProtKB/Swiss-Prot for OMD Gene
May be implicated in biomineralization processes. Has a function in binding of osteoblasts via the alpha(V)beta(3)-integrin (By similarity).