Skip to main content
. 2017 Nov 16;12(11):e0187926. doi: 10.1371/journal.pone.0187926

Table 1. Association of mouse knockout phenotypes with rare variants in CNR1 and DAGLA.

Gene* Phenotype Cases Controls OR P-value
CNR1 Pain sensitivity 9/22 156/950 3.5 0.036
CNR1 Anxiety 7/22 122/950 3.2 0.131
CNR1 Memory disorder 3/22 1/950 150 0.0003
CNR1 Sleep disorder 6/22 33/950 10.4 0.001
CNR1 Urinary frequency 2/22 19/950 4.9 0.301
CNR1 Seizures 11/22 402/950 1.4 1.000
CNR1 Hearing loss 1/22 31/950 1.4 1.000
CNR1 Pain sensitivity and anxiety 5/22 47/950 5.7 0.030
CNR1 Sleep disorder and anxiety 4/22 8/950 26.2 0.001
CNR1 Pain sensitivity and memory disorder 3/22 1/950 150 0.000
CNR1 Pain sensitivity, memory and sleep disorder 3/22 1/950 150 0.000
CNR1 Pain sensitivity, anxiety and memory disorder 2/22 0/950 N/A 0.003
CNR1 Pain sensitivity, anxiety, memory and sleep disorder 2/22 0/950 N/A 0.003
CNR1 Pain sensitivity and sleep disorder 3/22 7/950 21.3 0.005
DAGLA Anxiety 2/35 177/950 0.26 0.211
DAGLA Neurodevelopmental disorder 27/35 448/950 3.78 0.001
DAGLA Anxiety and neurodevelopmental disorder 2/35 98/950 0.53 1.000
DAGLA Seizures 30/35 595/950 3.84 0.032
DAGLA Seizures and neurodevelopmental disorder 22/35 332/950 3.15 0.003

*For each gene, the phenotypes that were evaluated are listed along with the number of cases or controls in which that phenotype was present out of the total number. Also listed are the odds ratio (OR), and P-values corrected for multiple testing. Confidence intervals for the odds ratios are provided in an extended version of the table in the supporting information (S7 Table).