3ff14cf26bd148e6bcf80df13e6b8c0b4c5da165
lrnassar
  Mon May 26 01:05:46 2025 -0700
Clarifying desc page, we no longer have missing genes except for those with version numbers <.99. Refs #35757

diff --git src/hg/makeDb/trackDb/human/panelApp.html src/hg/makeDb/trackDb/human/panelApp.html
index 1a8b5b0f5e0..284a886997d 100644
--- src/hg/makeDb/trackDb/human/panelApp.html
+++ src/hg/makeDb/trackDb/human/panelApp.html
@@ -16,42 +16,41 @@
 achieving consensus on gene panels in the <a target="_blank"
     href="https://www.england.nhs.uk/genomics/nhs-genomic-med-service/"> NHS
     Genomic Medicine Service (GMS)</a>. Later, the same platform was also deployed by
 <a target=_blank
    href="https://www.australiangenomics.org.au/tools-and-resources/panelapp-australia/">Australian
    Genomics</a>.
 </p>
 
 <p>
 <a href="https://panelapp.genomicsengland.co.uk/panels/entities/" target="_blank">Genes and genomic
 entities</a>, so short tandem repeats/STRs and copy number variants/CNVs,
 have been reviewed by experts to enable a community consensus to be reached on which
 genes and genomic entities should appear on a <b>diagnostics grade panel</b> for each disorder.
 A <b>rating system</b> (confidence level 0 - 3) is used to classify the level of evidence
 supporting association with phenotypes covered by the gene panel in question.
+Only PanelApp entries with a <b>version &gt; .99</b> are displayed in these tracks.
 </p>
 <p>
 There are six subtracks in total: Three different types (genes, STRs and CNVs) and these 
 three exist for both countries, England and Australia. The three types of tracks are:</p>
 
 <ul>
   <li>
     <b>PanelApp Genes (PanelApp Genes):</b>
     <br>
     shows genes with evidence supporting a gene-disease relationship.
-    <p style="color:red">NOTE: Due to a bug in the PanelApp gene API, between 
-       5 and 20% of gene entries are missing as of 11/2/22.</p>
 </li>
   <br>
   <li>
     <b>PanelApp STRs (PanelApp STRs):</b>
     <br>
     shows short tandem repeats that can be disease-causing when a particular number of repeats is
     present.</li>
   <br>
   <li>
     <b>Only on hg38: PanelApp Regions (PanelApp CNV Regions):</b>
     <br>
     shows copy-number variants (region-loss and region-gain) with evidence supporting a gene-disease
     relationship.</li>
 </ul>