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. Author manuscript; available in PMC: 2021 Aug 1.
Published in final edited form as: J Comp Neurol. 2020 Feb 19;528(12):2099–2131. doi: 10.1002/cne.24879

Figure 9. Structure of gene lists.

Figure 9.

(a) View of the organization and layout of a typical list of genes associated with a specific ZEBrA portal theme. In this example, a subset of genes associated with the Neurological/Psychiatric Disorder Epilepsy within the Human Diseases sub-portal is shown. Each gene entry includes a magnifying glass icon under the View In Situ column (which provides access to in situ images in the Image browser), and entries for gene name (which provides access to the Gene Info page), Gene Description, Attributes, and Linkouts (which in this case provide access to an entry in OMIM). (b-c) Views of example pop-up menus showing Attributes associated with the gene RELN that are derived from the Disease and Phenotypes (b) and Speech and Language (c) portals. The association of RELN with the OMIM Attribute “Epilepsy, familial temporal lobe, 7” provides the reasoning behind the classification of this gene under the Human Disease theme of Epilepsy.