<p>Tet family methylcytosine dioxygenases recognize and oxidize 5-methyl-cytosine (5mC) to 5-hydroxymethylcytosine (5hmC). Previous work demonstrated the requirement for Tet and 5hmC during zebrafish retinogenesis. <i>tet2</i>^{<i>−/−</i>}<i>;tet3</i>^{<i>−/−</i>} mutants possessed defects in the formation of differentiated retinal neurons, but the mechanisms underlying these defects are unknown. Here, we leveraged scRNAseq technologies to better understand cell type-specific deficits and molecular signatures underlying the <i>tet2</i>^{<i>−/−</i>}<i>;tet3</i>^{<i>−/−</i>} retinal phenotype. Our results identified defects in <i>tet2</i>^{<i>−/−</i>}<i>;tet3</i>^{<i>−/−</i>} retinae that included delayed specification of several retinal cell types, reduced maturity across late-stage cones, expansions of immature subpopulations of horizontal and bipolar cells, and altered biases of bipolar cell subtype fates at late differentiation stages. Together, these data highlight the critical role that tet2 and tet3 play as regulators of cell fate specification and terminal differentiation events during retinal development.</p>