Fundamental to our understanding about the function of the visual system is a basic knowledge of the structural components of neurons that comprise the circuit. The goal of the work described here aims to elucidate the structural, developmental, and molecular architecture of retinal ganglion cells (RGCs), using the mouse as a model system. I address three fundamental questions regarding synaptic specificity. First, do RGCs, whose dendrites are hallmarks of laminar specificity within the retina, also display laminar specificity of their axon terminals in the brain? To test this, I survey the axon terminal morphologies of different RGC subtypes and show that much like their dendrites, the axon terminals also display laminar specificity within the superior colliculus (SC). Second, what are the structural changes that take place over development that result in targeting of RGC axons to their proper target cells in the dorsal lateral geniculate (dLGN)? By observing the structural development of a single subtype of RGC I demonstrate that, in the retinogeniculate system, a dominant mechanism of synapse refinement is the growth and redistribution of synapses along the axon arbor. Finally, what are the molecular mechanisms that mediate laminar specificity? Sidekicks are synaptic cell adhesion molecules that are thought to mediate laminar specificity of dendrites in the chick retina. Functional studies would benefit from using mice, where genetic tools are more readily available. I show that Sidekick1 and 2 are localized to restricted sublaminae within the mouse retina, and is also present in other sensory neurons. The expression analysis is a necessary first step, and sets the foundation for studying the functional role of Sidekicks in ongoing work with loss-of-function mouse models.