Results of analyses can be viewed either at a single transcript looking at all linked phenotypes, or for a single phenotype looking at all linked transcripts.
The results allow a user to quickly identify potential phenotypic consequences of loss-of-function in a gene, or to identify which genes are linked to a specified phenotype of interest.
Search by gene, transcript ID, or analysis using the options in the left hand menu (figure 1).
Figure 1: Transcript variant set analysis search options.
Check or amend your release settings
Prior to loading your data of interest, check the pre-selected data release, or select the required release using the release selection options. Also check the Ensembl reference used by the dataset (e.g. GRCh38).
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