ff4257af63b8ef729573df54c879eb05876b26ed
dschmelt
  Wed Nov 2 10:51:48 2022 -0700
Adding note about the bug in refs# 30212

diff --git src/hg/makeDb/trackDb/human/panelApp.html src/hg/makeDb/trackDb/human/panelApp.html
index 9508b66..93cf20b 100644
--- src/hg/makeDb/trackDb/human/panelApp.html
+++ src/hg/makeDb/trackDb/human/panelApp.html
@@ -16,31 +16,34 @@
 <a href="https://panelapp.genomicsengland.co.uk/panels/entities/" target="_blank">Genes and genomic
 entities</a> (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.
 </p>
 <p>
 The available data tracks are: 
 </p>
 
 <ul>
   <li>
     <b>Genomics England PanelApp Genes (PanelApp Genes):</b>
     <br>
-    shows genes with evidence supporting a gene-disease relationship.</li>
+    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>Genomics England 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: Genomics England 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>
 
 <h2>Display Conventions</h2>