coffin-siris syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A genetic disease that is characterized by underdevelopment of the tips of fingers or toes, underdevelopment or abscense of finger or toe nails and developmental disability. (Human Disease Ontology, DOID_1925)
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Genes

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

Symbol Name Standardized Value
ARID1B AT rich interactive domain 1B (SWI1-like) 2.47211
SMARCE1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 2.2889
PHF6 PHD finger protein 6 1.97457
ARID1A AT rich interactive domain 1A (SWI-like) 1.81284
CPED1 cadherin-like and PC-esterase domain containing 1 1.74642
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1 1.71134
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 1.70269
TBC1D24 TBC1 domain family, member 24 1.64936
BANF1 barrier to autointegration factor 1 1.60368
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 1.37469
SOX11 SRY (sex determining region Y)-box 11 1.20959
LAX1 lymphocyte transmembrane adaptor 1 1.15496
FAM3C family with sequence similarity 3, member C 1.12319
WNT16 wingless-type MMTV integration site family, member 16 1.11477
ADNP activity-dependent neuroprotector homeobox 0.904854
NIPBL Nipped-B homolog (Drosophila) 0.732596
PAX6 paired box 6 0.357077