The ganglionic eminence (GE) is a transitory structure in the development of the nervous system that guides cell and axon migration. It is present in the embryonic and fetal stages of neural development found between the thalamus and caudate nucleus.

The eminence is divided into three regions of the ventral ventricular zone of the telencephalon (a lateral, medial and caudal eminence), where they facilitate tangential cell migration during embryonic development. Tangential migration does not involve interactions with radial glial cells; instead the interneurons migrate perpendicularly through the radial glial cells to reach their final location. The characteristics and function of the cells that follow the tangential migration pathway seem to be closely related to the location and precise timing of their production, and the GEs contribute significantly to building up the GABAergic cortical cell population. Another structure that the GEs contribute to is the basal ganglia. The GEs also guide the axons growing from the thalamus into the cortex and vice versa.

In humans, the GEs disappear by one year of age. During development, neuronal migration continues until the extinction of the germ layer, at which point the remnants from the germ layer make up the eminences.

Ganglionic eminences are categorized into three groups based on their location within the subventricular zone:

A sulcus separates the medial and lateral ganglionic eminences. The expression of Nkx2-1, Gsx2, and Pax6 is required to determine the independent progenitor cell populations in the LGE and MGE. Interactions between these three genes define the boundaries between the different progenitor zones and mutations of these genes can cause abnormal expansion around the MGE, LGE, ventral pallium (VP), and anterior entopeduncular region (AEP). The cells of the GEs are quite homogenous, with the MGE, LGE, and CGE all having small, dark, irregular nuclei and moderately dense cytoplasm, however, each eminence can be identified by the type of progeny that it produces. See the individual GE sections below for more information on the different types of progeny produced.

Additionally, the subventricular zone is the starting point of multiple streams of tangentially migrating interneurons that express Dlx genes. There are three main tangential migration pathways that have been identified in this region:

These pathways are temporally and spatially distinct, and produce a variety of GABAergic, and non-GABAergic interneurons. One example of GABAergic interneurons that the GEs guide are parvalbumin-containing interneurons in the neocortex. Some examples of non-GABAergic interneurons that the GEs guide are dopaminergic interneurons in the olfactory bulb, and cholinergic interneurons in the striatum. Cells migrating along these pathways move at different rates. Some molecules that have been implicated in controlling the rate of the unidirectional movement of cells derived from the GEs are hepatocyte growth factor/scattered factor (HGF/SF), and various neurotrophic factors.

The primary purpose of the MGE during development is to produce GABAergic stellate cells and direct their migration to the neocortex. The precursors of most GABAergic interneurons in the cerebral cortex migrate from the subcortical progenitor zone. More specifically, performing a mechanical transection of the migratory route from the MGE to the neocortex causes a 33% decrease in GABAergic interneurons in the neocortex. The MGE also produces some of the neurons and glia of the basal ganglia and hippocampus. The MGE may also be a source of Cajal-Retzius cells, but this remains controversial. Early in embryonic development, the interneurons in the cortex stem primarily from the MGE and the AEP. In vitro experiments show that MGE cells migrate more than 300 μm per day, three times faster than the migration of LGE cells. See more about the time frame and function of MGE in comparison to the LGE in the following section.