paralytic ileus Gene Set

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

36 genes co-occuring with the disease paralytic ileus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
DNAJC15 DnaJ (Hsp40) homolog, subfamily C, member 15 1.07866
AVP arginine vasopressin 0.875329
CFAP74 cilia and flagella associated protein 74 0.795821
ACAP3 ArfGAP with coiled-coil, ankyrin repeat and PH domains 3 0.794181
RAMP1 receptor (G protein-coupled) activity modifying protein 1 0.785984
CCK cholecystokinin 0.707559
SNRPD1 small nuclear ribonucleoprotein D1 polypeptide 16kDa 0.685491
CALCRL calcitonin receptor-like 0.673518
IGHV1-2 immunoglobulin heavy variable 1-2 0.660404
CNR1 cannabinoid receptor 1 (brain) 0.590558
TP73 tumor protein p73 0.580439
ALB albumin 0.544318
NOS1 nitric oxide synthase 1 (neuronal) 0.533088
BCHE butyrylcholinesterase 0.528449
NDUFS7 NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase) 0.477909
CELA1 chymotrypsin-like elastase family, member 1 0.465038
OR10T2 olfactory receptor, family 10, subfamily T, member 2 0.461639
CELA3B chymotrypsin-like elastase family, member 3B 0.455224
IARS isoleucyl-tRNA synthetase 0.442418
MLN motilin 0.43941
TACR1 tachykinin receptor 1 0.387423
IL6 interleukin 6 0.375179
IL6R interleukin 6 receptor 0.35892
TYMP thymidine phosphorylase 0.27687
TRPV1 transient receptor potential cation channel, subfamily V, member 1 0.275089
EDA ectodysplasin A 0.267622
CRP C-reactive protein, pentraxin-related 0.266558
INS insulin 0.24996
PRRC2A proline-rich coiled-coil 2A 0.23945
AAAS achalasia, adrenocortical insufficiency, alacrimia 0.234225
CD22 CD22 molecule 0.232142
NOS2 nitric oxide synthase 2, inducible 0.213283
CBS cystathionine-beta-synthase 0.208579
AQP4 aquaporin 4 0.182957
ASRGL1 asparaginase like 1 0.175679
SST somatostatin 0.171785