(GWAS data used on the Zebrafish Mutation Project Web site comes from

Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.

The human homologues of the following genes have been identified in this study:

Gene name Reported Gene Ensembl ID Alleles found Associated phenotype Study Count
foxo1a FOXO1 ENSDARG00000063540 1 Not determined 3
foxo1b FOXO1 ENSDARG00000061549 1 Not determined 3

The following reported genes could not be linked automatically to a zebrafish gene:

  • ZNF469