032f71725a8af7b83496a5fef12ca0f1123cbead
lrnassar
  Tue Apr 15 16:39:19 2025 -0700
Squashing stale pennanticons.

diff --git src/hg/makeDb/trackDb/human/trackDb.clinGen.ra src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
index 284efc4e1ef..1e502ddc6f2 100644
--- src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
+++ src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
@@ -1,72 +1,70 @@
 track clinGenComp
 shortLabel ClinGen
 longLabel ClinGen curation activities (Dosage Sensitivity and Gene-Disease Validity)
 visibility hide
 type bigBed 9 +
 group phenDis
 itemRgb on
 compositeTrack on
 noParentConfig on
 html clinGen
-pennantIcon New red ../goldenPath/newsarch.html#100924 "October 9, 2024"
 
     track clinGenHaplo
     showCfg on
     priority 1
     parent clinGenComp on
     shortLabel ClinGen Haploinsufficiency
     longLabel ClinGen Dosage Sensitivity Map - Haploinsufficiency
     visibility pack
     type bigBed 9 +
     bigDataUrl /gbdb/$D/bbi/clinGen/clinGenHaplo.bb
     mouseOverField _mouseOver
     filterValues.haploScore 0|No evidence available,1|Little evidence for dosage pathogenicity,2|Some evidence for dosage pathogenicity,3|Sufficient evidence for dosage pathogenicity,30|Gene associated with autosomal recessive phenotype,40|Dosage sensitivity unlikely
     filterLabel.haploScore Dosage Sensitivity Score
     urls url="$$" PMID1="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID2="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID3="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID4="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID5="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID6="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" mondoID="https://monarchinitiative.org/disease/$$"
 
     track clinGenTriplo
     priority 2
     parent clinGenComp on
     shortLabel ClinGen Triplosensitivity
     longLabel ClinGen Dosage Sensitivity Map - Triplosensitivity
     visibility pack
     type bigBed 9 +
     bigDataUrl /gbdb/$D/bbi/clinGen/clinGenTriplo.bb
     mouseOverField _mouseOver
     filterValues.triploScore 0|No evidence available,1|Little evidence for dosage pathogenicity,2|Some evidence for dosage pathogenicity,3|Sufficient evidence for dosage pathogenicity,30|Gene associated with autosomal recessive phenotype,40|Dosage sensitivity unlikely
     filterLabel.triploScore Dosage Sensitivity Score
     urls url="$$" PMID1="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID2="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID3="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID4="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID5="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" PMID6="https://pubmed.ncbi.nlm.nih.gov/$$/?from_single_result=$$&expanded_search_query=$$" mondoID="https://monarchinitiative.org/disease/$$"
 
     track clinGenGeneDisease
     priority 3
     parent clinGenComp on
     type bigBed 9 +
     shortLabel ClinGen Validity
     longLabel ClinGen Gene-Disease Validity Classification
     bigDataUrl /gbdb/$D/bbi/clinGen/clinGenGeneDisease.bb
     visibility pack
     mouseOverField Mouseover
     urls geneSymbol="https://search.clinicalgenome.org/kb/genes/$$" ClinGenURL="https://search.clinicalgenome.org/kb/gene-validity/$$" HGNCid="https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/$$" MONDOid="https://monarchinitiative.org/disease/$$"
     skipFields Mouseover
     sepFields MONDOid,SOPversion
     itemRgb on
     noScoreFilter on
     searchIndex name,geneSymbol,HGNCid,MONDOid,Classification
     filterValues.Inheritance Autosomal Dominant,Autosomal Recessive,Semidominant,X-Linked,X-linked recessive,Other
     filterLabel.Inheritance Inheritance Pattern
     filterValues.SOPversion SOP4,SOP5,SOP6,SOP7
     filterLabel.SOPversion ClinGen SOP Version Number
     filterValues.Classification Definitive,Strong,Moderate,Limited,Animal Model Only,No Reported Evidence,Disputed,Refuted
     filterLabel.Classification ClinGen Gene-Disease Validity Classification
     bedNameLabel Associated Disease
 
     track clinGenCspec
     shortLabel ClinGen VCEP Specifications
     longLabel Clingen CSpec Variant Interpretation VCEP Specifications
     parent clinGenComp on
     noScoreFilter on
     type bigBed 9 +
     bigDataUrl /gbdb/$D/bbi/clinGen/clinGenCspec.bb
     visibility pack
     mouseOver <b>Disease:</b> $disease <br><b>Panel:</b> $panel <br><b>Status:</b> $status
-    pennantIcon New red ../goldenPath/newsarch.html#100924 "October 9, 2024"