48578d7724625cda2499bd11f8b6ce19463a1279
braney
  Fri Sep 2 15:24:25 2022 -0700
HGNC track is ready for QA.

diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra
index bb21f61..10928e7 100644
--- src/hg/makeDb/trackDb/human/trackDb.ra
+++ src/hg/makeDb/trackDb/human/trackDb.ra
@@ -5605,30 +5605,33 @@
 type bigBed 9 +
 bedNameLabel OrphaCode
 url http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=$$
 urlLabel OrphaNet Phenotype Link:
 urls ensemblID="https://grch37.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=$$" pmid="https://pubmed.ncbi.nlm.nih.gov/$$" orphaCode="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=$$" omim="https://www.omim.org/entry/$$?search=$$&highlight=$$" hgnc="https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/HGNC:$$"
 skipEmptyFields on
 skipFields name,score,itemRgb
 mouseOver Gene: $geneSymbol, Disorder: $disorder, Inheritance(s): $inheritance, Onset: $onsetList
 filterValues.assnType Biomarker tested in,Candidate gene tested in,Disease-causing germline mutation(s) (gain of function) in,Disease-causing germline mutation(s) (loss of function) in,Disease-causing germline mutation(s) in,Disease-causing somatic mutation(s) in,Major susceptibility factor in,Modifying germline mutation in,Part of a fusion gene in,Role in the phenotype of
 filterValues.inheritance Autosomal dominant,Autosomal recessive,Mitochondrial inheritance,Multigenic/multifactorial,No data available,Not applicable,Oligogenic,Semi-dominant,Unknown,X-linked dominant,X-linked recessive,Y-linked
 filterValues.onsetList Adolescent,Adult,All ages,Antenatal,Childhood,Elderly,Infancy,Neonatal,No data available
 itemRgb on
 
 track hgnc
 shortLabel HGNC
-longLabel HGNC
+longLabel HUGO Gene Nomenclature 
 bigDataUrl /gbdb/$D/hgnc/hgnc.bb
 type bigBed 9 +
 labelFields symbol, geneName, name, uniprot_ids, ensembl_gene_id, ucsc_id, refseq_accession
 defaultLabelFields symbol
 mouseOver Symbol:$symbol; $name, Alias symbol: $alias_symbol; Previous symbols:$prev_symbol
 filterValues.locus_type RNA Y,RNA cluster,RNA long non-coding,RNA micro,RNA misc,RNA ribosomal,RNA small nuclear,RNA small nucleolar,RNA transfer,RNA vault,T cell receptor gene,T cell receptor pseudogene,complex locus constituent,endogenous retrovirus,fragile site,gene with protein product,immunoglobulin gene,immunoglobulin pseudogene,locus_type,protocadherin,pseudogene,readthrough,region,unknown,virus integration site,
 group genes
 searchIndex name
 searchTrix /gbdb/$D/hgnc/search.ix
+skipEmptyFields on
+itemRgb on
+noScoreFilter on
 
 searchTable hgnc
 searchMethod exact
 searchType bigBed