The tuberal hypothalamus is comprised of the dorsomedial, ventromedial, and arcuate nuclei, as well as parts of the lateral hypothalamic area, and it governs a wide range of physiologies. During neurogenesis, tuberal hypothalamic neurons are thought to be born in a dorsal-to-ventral and outside-in pattern, although the accuracy of this description has been questioned over the years. Moreover, the intrinsic factors that control the timing of neurogenesis in this region are poorly characterized. Proneural genes, includingAchate-scute-like 1(Ascl1) andNeurogenin 3(Neurog3) are widely expressed in hypothalamic progenitors and contribute to lineage commitment and subtype-specific neuronal identifies, but the potential role of Neurogenin 2 (Neurog2) remains unexplored. Birthdating in male and female mice showed that tuberal hypothalamic neurogenesis begins as early as E9.5 in the lateral hypothalamic and arcuate and rapidly expands to dorsomedial and ventromedial neurons by E10.5, peaking throughout the region by E11.5. We confirmed an outside-in trend, except for neurons born at E9.5, and uncovered a rostrocaudal progression but did not confirm a dorsal-ventral patterning to tuberal hypothalamic neuronal birth. In the absence ofNeurog2, neurogenesis stalls, with a significant reduction in early-born BrdU+cells but no change at later time points. Further, the loss ofAscl1yielded a similar delay in neuronal birth, suggesting thatAscl1cannot rescue the loss ofNeurog2and that these proneural genes act independently in the tuberal hypothalamus. Together, our findings show thatNeurog2functions as a classical proneural gene to regulate the temporal progression of tuberal hypothalamic neurogenesis.SIGNIFICANCE STATEMENTHere, we investigated the general timing and pattern of neurogenesis within the tuberal hypothalamus. Our results confirmed an outside-in trend of neurogenesis and uncovered a rostrocaudal progression. We also showed thatNeurog2acts as a classical proneural gene and is responsible for regulating the birth of early-born neurons within the ventromedial hypothalamus, acting independently ofAscl1. In addition, we revealed a role forNeurog2in cell fate specification and differentiation of ventromedial -specific neurons. Last,Neurog2does not have cross-inhibitory effects onNeurog1,Neurog3, andAscl1. These findings are the first to reveal a role forNeurog2in hypothalamic development.