weaver syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_14731)
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Genes

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

Symbol Name Standardized Value
PNPLA8 patatin-like phospholipase domain containing 8 2.14737
CTTNBP2 cortactin binding protein 2 1.78759
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit 1.49745
NUP98 nucleoporin 98kDa 1.22779
NRCAM neuronal cell adhesion molecule 1.03409
KMT2B lysine (K)-specific methyltransferase 2B 0.990644
SETD2 SET domain containing 2 0.947019
GALNS galactosamine (N-acetyl)-6-sulfatase 0.891718
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like 0.839705
EP300 E1A binding protein p300 0.824538
MFN2 mitofusin 2 0.750864
ASXL1 additional sex combs like transcriptional regulator 1 0.741517
GPC3 glypican 3 0.603811
TH tyrosine hydroxylase 0.593285
HIST2H3PS2 histone cluster 2, H3, pseudogene 2 0.406798
H3F3A H3 histone, family 3A 0.40008
H3F3B H3 histone, family 3B (H3.3B) 0.40008
NF1 neurofibromin 1 0.243295