83077bd03336bc37132962d741d69bff0f5a741d
abenetpa
  Fri Sep 25 01:57:36 2020 -0700
changed long track name refs #24818

diff --git src/hg/makeDb/trackDb/human/trackDb.clinGen.ra src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
index 89350ed..1f91da8 100644
--- src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
+++ src/hg/makeDb/trackDb/human/trackDb.clinGen.ra
@@ -1,61 +1,61 @@
 track clinGenComp
 shortLabel ClinGen
-longLabel Clinical Genome Resource (ClinGen) Dosage Sensitivity Map
+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#092320 "Released Sep. 23, 2020"
 
     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=$$&expanded_search_query=$$" omimID="https://omim.org/entry/$$"
 
     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=$$&expanded_search_query=$$" omimID="https://omim.org/entry/$$"
 
     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 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 score,strand,thickStart,thickEnd,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