partington syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

16 genes co-occuring with the disease partington syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ARX aristaless related homeobox 2.65701
DLG3 discs, large homolog 3 (Drosophila) 1.71545
PQBP1 polyglutamine binding protein 1 1.13501
OPHN1 oligophrenin 1 1.1051
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3 1.08705
NKX2-2 NK2 homeobox 2 0.986007
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter) 0.955779
ASCL1 achaete-scute family bHLH transcription factor 1 0.801974
AFF2 AF4/FMR2 family, member 2 0.776568
SKP1 S-phase kinase-associated protein 1 0.74883
PNLIP pancreatic lipase 0.733001
ATRX alpha thalassemia/mental retardation syndrome X-linked 0.71925
MNX1 motor neuron and pancreas homeobox 1 0.502675
MECP2 methyl CpG binding protein 2 0.476772
PPY pancreatic polypeptide 0.411283
GHRL ghrelin/obestatin prepropeptide 0.331025