Several genes have been associated with the mendelian forms of early-onset glaucoma: defects in the myocilin gene (GLC1A) primarily cause elevated pressure [1,2], the optineurin gene (GLC1E), appears to contribute to disease in familial low tension glaucoma [3-5]; and the WDR36 gene (GLC1G) may be a modifier gene that influences the severity of the glaucoma phenotype [6,7]. This evidence concerns the gene WDR36 and glaucoma.