a224faf89971608c75cd3c91ddc797da891bef2c lrnassar Thu Feb 2 16:48:01 2023 -0800 Adding more info in mouseOver requested by Ana, no RM. diff --git src/hg/makeDb/trackDb/human/genCC.html src/hg/makeDb/trackDb/human/genCC.html index 1085322..da2f4fe 100644 --- src/hg/makeDb/trackDb/human/genCC.html +++ src/hg/makeDb/trackDb/human/genCC.html @@ -12,31 +12,32 @@ The GenCC aims to clarify overlap between gene curation efforts and develop consistent terminology for validity, allelic requirement and mechanism of disease. Each item on this track corresponds with a gene, and contains a large number of information such as associated disease, evidence classification, specific submission notes and identifiers from different databases. In cases where multiple annotations exist for the same gene, multiple items are displayed.</p> <h2>Display Conventions and Configuration</h2> <p> Each item displayed represents a submission to the GenCC database. The displayed name is a combination of the gene symbol and the disease's original submission ID. This submission ID is either the OMIM#, MONDO# or Orphanet#. Clicking on any item will display the complete meta data for that item, including linkouts to the GenCC, NCBI, Ensembl, HGNC, GeneCards, Pombase (MONDO), and Human Phenotype Ontology (HPO). Mousing over any item will display the -associated disease for that submission.</p> +associated disease title, the classification title, and the mode of inheritance +title.</p> <p> Items are colored based on the GenCC classification, or validation, of the evidence in the color scheme seen in the table below. For more information on this process, see the <a target="_blank" href="https://thegencc.org/faq.html#validity-termsdelphi-survey">GenCC validity terms FAQ</a>. A filter for the track is also available to display a subset of the items based on their classification.</p> <p> <table cellpadding='2'> <thead><tr> <th style="border-bottom: 2px solid;">Color</th> <th style="border-bottom: 2px solid;">Evidence classification</th> </tr></thead>