urethral intrinsic sphincter deficiency Gene Set

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

19 genes co-occuring with the disease urethral intrinsic sphincter deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MEOX2 mesenchyme homeobox 2 1.87377
LPP LIM domain containing preferred translocation partner in lipoma 1.58046
PURA purine-rich element binding protein A 1.31668
PARP15 poly (ADP-ribose) polymerase family, member 15 1.26298
MYBPC1 myosin binding protein C, slow type 1.05387
NPR1 natriuretic peptide receptor 1 0.857315
GUCY2C guanylate cyclase 2C 0.856087
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family) 0.849536
GPER1 G protein-coupled estrogen receptor 1 0.815514
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary) 0.663975
MAOA monoamine oxidase A 0.542379
PIDD1 p53-induced death domain protein 1 0.526518
KIAA0101 KIAA0101 0.491978
VIP vasoactive intestinal peptide 0.39598
IGF1R insulin-like growth factor 1 receptor 0.325916
GLB1 galactosidase, beta 1 0.28294
BCR breakpoint cluster region 0.280082
MB myoglobin 0.261245
ALPP alkaline phosphatase, placental 0.224884