roberts 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_5325)
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Genes

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

Symbol Name Standardized Value
ESCO1 establishment of sister chromatid cohesion N-acetyltransferase 1 2.70093
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2 2.68146
CDCA5 cell division cycle associated 5 2.04596
SMC3 structural maintenance of chromosomes 3 1.79976
ABT1 activator of basal transcription 1 1.65655
ZW10 zw10 kinetochore protein 1.58136
NIPBL Nipped-B homolog (Drosophila) 1.43771
ZWINT ZW10 interacting kinetochore protein 1.41972
ZNF143 zinc finger protein 143 1.34286
RAD21 RAD21 homolog (S. pombe) 1.31886
INCENP inner centromere protein antigens 135/155kDa 1.25994
DDX11 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11 1.21089
DDX11L8 DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11 like 8 1.21089
SMC1A structural maintenance of chromosomes 1A 0.975482
SGOL1 shugoshin-like 1 (S. pombe) 0.918024
MKKS McKusick-Kaufman syndrome 0.847898
BRIP1 BRCA1 interacting protein C-terminal helicase 1 0.712796
SERPINA6 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 6 0.58433
EIF4EBP1 eukaryotic translation initiation factor 4E binding protein 1 0.420641
MNX1 motor neuron and pancreas homeobox 1 0.379256
ERCC2 excision repair cross-complementation group 2 0.327375
RUNX1 runt-related transcription factor 1 0.319726