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. 2021 Dec 24;9:769409. doi: 10.3389/fcell.2021.769409

TABLE 1.

Top 24 enriched diseases of 44 HP-MRGs analyzed with the Comparative Toxicogenomics Database.

Disease name Disease categories p-value Corrected p-value Annotated genes quantity Annotated genes Genome frequency
Metabolism, inborn errors Genetic disease (inborn)|metabolic disease 3.37E-12 1.09E-09 12 AGPAT2|APRT|ASS1|GSS|IDH2|ITPA|LDHB|OGDH|OPLAH|PC|PDHB|PMM2 706/44146 genes: 1.60%
Nutritional and metabolic diseases 3.17E-11 1.02E-08 15 AGPAT2|APRT|ASS1|CA3|ENTPD6|GSS|IDH2|ITPA|LDHB|OGDH|OPLAH|PC|PDHB|PIK3CA|PMM2 1656/44146 genes: 3.75%
Pathological conditions, signs, and symptoms 1.4E-09 4.53E-07 18 AKR1B1|ALOX15|BDH1|BLVRA|CA3|CANT1|DGKZ|ENTPD2|ENTPD6|GMPPA|GPX2|IDH2|ITPA|LDHB|PAFAH1B1|PC|PIK3CA|PMM2 3421/44146 genes: 7.75%
Metabolic diseases Metabolic disease 2.04E-09 6.59E-07 13 AGPAT2|APRT|ASS1|GSS|IDH2|ITPA|LDHB|OGDH|OPLAH|PC|PDHB|PIK3CA|PMM2 1540/44146 genes: 3.49%
Genetic diseases, inborn Genetic disease (inborn) 2.55E-09 8.22E-07 15 AGPAT2|APRT|ASS1|CANT1|GMPPA|GSS|IDH2|ITPA|LDHB|OGDH|OPLAH|PC|PDHB|PIK3CA|PMM2 2275/44146 genes: 5.15%
Congenital, hereditary, and neonatal diseases and abnormalities 8.69E-09 2.81E-06 16 AGPAT2|APRT|ASS1|CANT1|GMPPA|GSS|IDH2|ITPA|LDHB|OGDH|OPLAH|PAFAH1B1|PC|PDHB|PIK3CA|PMM2 2912/44146 genes: 6.60%
Pathologic processes Pathology (process) 3.42E-08 1.11E-05 14 AKR1B1|BDH1|BLVRA|CA3|CANT1|DGKZ|ENTPD2|GPX2|IDH2|ITPA|LDHB|PAFAH1B1|PC|PIK3CA 2342/44146 genes: 5.31%
Digestive system diseases Digestive system disease 3.99E-08 1.29E-05 15 AKR1B1|ALOX15|ASS1|BDH1|BLVRA|CA3|DGAT2|ENTPD2|GMPPA|GPX2|LDHB|OGDH|PC|PIK3CA|PMM2 2793/44146 genes: 6.33%
Liver diseases Digestive system disease 3.25E-07 0.000105 12 AKR1B1|ASS1|BDH1|BLVRA|CA3|DGAT2|ENTPD2|GPX2|LDHB|OGDH|PC|PIK3CA 1964/44146 genes: 4.45%
Neoplasms Cancer 1.7E-06 0.00055 15 AKR1B1|ALOX15|APRT|DEGS1|ENTPD6|GPX2|GSS|IDH2|LDHB|PAFAH1B1|PC|PDHB|PIK3CA|PMM2|PYGB 3736/44146 genes: 8.46%
Carcinoma, renal cell Cancer|urogenital disease (female)|urogenital disease (male) 9.17E-06 0.00296 4 APRT|LDHB|PDHB|PIK3CA 131/44146 genes: 0.30%
Amino acid metabolism, inborn errors Genetic disease (inborn)|metabolic disease 1.33E-05 0.0043 4 ASS1|GSS|OGDH|OPLAH 144/44146 genes: 0.33%
Liver cirrhosis Digestive system disease|pathology (process) 2.74E-05 0.00885 7 AKR1B1|BDH1|BLVRA|CA3|ENTPD2|LDHB|PC 895/44146 genes: 2.03%
Kidney neoplasms Cancer|urogenital disease (female)|urogenital disease (male) 4.11E-05 0.01327 4 APRT|LDHB|PDHB|PIK3CA 192/44146 genes: 0.43%
Fibrosis Pathology (process) 4.19E-05 0.01354 7 AKR1B1|BDH1|BLVRA|CA3|ENTPD2|LDHB|PC 957/44146 genes: 2.17%
Brain diseases, metabolic, inborn Genetic disease (inborn)|metabolic disease|nervous system disease 0.000052 0.0168 4 ASS1|IDH2|PC|PDHB 204/44146 genes: 0.46%
Chemical and drug-induced liver injury Digestive system disease 5.44E-05 0.01756 5 BDH1|CA3|DGAT2|OGDH|PC 410/44146 genes: 0.93%
Kidney diseases Urogenital disease (female)|urogenital disease (male) 5.98E-05 0.01931 6 APRT|DGKH|IDH2|LDHB|PDHB|PIK3CA 688/44146 genes: 1.56%
Brain diseases, metabolic Metabolic disease|nervous system disease 9.14E-05 0.02951 4 ASS1|IDH2|PC|PDHB 236/44146 genes: 0.53%
Diabetes complications Endocrine system disease 0.000109 0.03522 3 AKR1B1|ASS1|DGKH 92/44146 genes: 0.21%
Pyruvate metabolism, inborn errors Genetic disease (inborn)|metabolic disease 0.000115 0.0373 2 PC|PDHB 16/44146 genes: 0.04%
Liver cirrhosis, experimental Digestive system disease|pathology (process) 0.000116 0.03761 6 AKR1B1|BDH1|BLVRA|CA3|LDHB|PC 777/44146 genes: 1.76%
Neoplasms by site Cancer 0.000117 0.03763 11 AKR1B1|ALOX15|APRT|DEGS1|GPX2|GSS|LDHB|PDHB|PIK3CA|PMM2|PYGB 2958/44146 genes: 6.70%
Neoplastic processes Cancer|pathology (process) 0.000133 0.04289 5 GPX2|IDH2|LDHB|PAFAH1B1|PIK3CA 496/44146 genes: 1.12%

HP-MRGs: Helicobacter pylori–associated metabolism-related genes.