Human Gene Set: WP_16P112_PROXIMAL_DELETION_SYNDROME


Standard name WP_16P112_PROXIMAL_DELETION_SYNDROME
Systematic name M40057
Brief description 16p11.2 proximal deletion syndrome
Full description or abstract  
Collection C2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP4949
Related gene sets  
External links https://www.wikipathways.org/instance/WP4949
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Source species Homo sapiens
Contributed by WikiPathways
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 76 genes
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Show members (show 76 source identifiers mapped to 76 genes)
Version history 2024.1.Hs: Renamed from WP_16P11_2_PROXIMAL_DELETION_SYNDROME. Updated to WikiPathways Release 20240710

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