Human Gene Set: WP_RETT_SYNDROME


Standard name WP_RETT_SYNDROME
Systematic name M39759
Brief description Rett syndrome
Full description or abstract  
Collection C2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP4312
Related gene sets  
External links https://www.wikipathways.org/instance/WP4312
Filtered by similarity ?
Source species Homo sapiens
Contributed by WikiPathways
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
Download gene set format: grp | gmt | xml | json | TSV metadata
Compute overlaps ? (show collections to investigate for overlap with this gene set)
Compendia expression profiles ? NG-CHM interactive heatmaps
(Please note that clustering takes a few seconds)
GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)

Legacy heatmaps (PNG)
GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 48 genes
Gene families ? Categorize these 48 genes by gene family
Show members (show 48 source identifiers mapped to 48 genes)
Version history 2024.1.Hs: Renamed from WP_RETT_SYNDROME_CAUSING_GENES. Updated to WikiPathways Release 20240710

See MSigDB license terms here. Please note that certain gene sets have special access terms.