sensenbrenner 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. [SN]. (Human Disease Ontology, DOID_0050577)
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Genes

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

Symbol Name Standardized Value
WDR35 WD repeat domain 35 2.72541
IFT43 intraflagellar transport 43 2.18659
TULP4 tubby like protein 4 2.11485
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1 1.92342
WDR19 WD repeat domain 19 1.91453
IFT80 intraflagellar transport 80 1.90056
IFT172 intraflagellar transport 172 1.71909
TTC21B tetratricopeptide repeat domain 21B 1.59564
IFT122 intraflagellar transport 122 1.58136
NEK1 NIMA-related kinase 1 1.46671
EVC2 Ellis van Creveld syndrome 2 1.24211
EVC Ellis van Creveld protein 1.11603
INSR insulin receptor 0.253479