Research Article

Comparative Transcriptome Analysis Reveals the Potential Cardiovascular Protective Targets of the Thyroid Hormone Metabolite 3-Iodothyronamine (3-T1AM)

Table 2

The 90 enriched genes associated with cardiovascular diseases analyzed with the Comparative Toxicogenomics Database.

Disease nameDisease categories valueCorrected valueAnnotated gene quantityAnnotated genesGenome frequency

Cardiovascular diseasesCardiovascular disease2.81-133.78-1090ANXA1|ATP7A|BRAF|CALM2|CALU|CAMK2D|CANX|CASP12|CASQ2|CCL2|COX1|COX2|COX3|CRBN|CXCL1|CYTB|des|DNM1L|EIF2A|ERAP1|FKBP14|FKTN|GAA|GATAD1|GLRX3|GSTA4|GSTT1|HIF1A|HMGB1|HMOX1|HSF2|HSPA9|HSPD1|JAK2|KLF13|KRAS|MAOA|MAPRE1|MEX3C|MFF|NCL|ND1|ND5|ND6|NDUFS1|NEDD4|NEXN|NF1|NR3C1|NR4A1|NRAS|NUCKS1|NUP155|PAK2|PDIA3|PON2|PPP2CA|PPP3R1|PROS1|PSEN2|PSMA2|PSMA6|PSMB7|PTP4A2|RASA1|RENBP|ROCK2|SCN1B|SGCA|SGCD|SHOC2|SIRT4|SLC4A3|STK39|TAP1|TBCA|TFPI|TFRC|TLL1|TNFAIP6|TRIM63|TRPM4|UFD1|UGCG|USP34|WDPCP|WDR12|WNK4|XPO1|YES11452/43293 genes: 3.35%

Heart diseasesCardiovascular disease7.42E-119.97E-0868BRAF|CALM2|CALU|CAMK2D|CANX|CASP12|CASQ2|CCL2|COX1|des|DNM1L|EIF2A|FKTN|GAA|GATAD1|GLRX3|HIF1A|HMGB1|HMOX1|HSF2|HSPA9|HSPD1|JAK2|KLF13|KRAS|MAPRE1|MEX3C|MFF|NCL|NDUFS1|NEDD4|NEXN|NF1|NR3C1|NR4A1|NRAS|NUCKS1|NUP155|PAK2|PDIA3|PPP2CA|PPP3R1|PSEN2|PSMA2|PSMA6|PSMB7|PTP4A2|RENBP|ROCK2|SCN1B|SGCA|SGCD|SHOC2|SIRT4|SLC4A3|TAP1|TBCA|TFRC|TLL1|TRIM63|TRPM4|UFD1|UGCG|USP34|WDPCP|WDR12|XPO1|YES11066/43293 genes: 2.46%

MELAS syndromeCardiovascular disease
|Genetic disease (inborn)
|Metabolic disease
|Musculoskeletal disease
|Nervous system disease
1.20E-060.001617COX1|COX2|COX3|CYTB|ND1|ND5|ND622/43293 genes: 0.05%

Vascular diseasesCardiovascular disease2.59E-060.0034850ANXA1|ATP7A|CAMK2D|CANX|CASP12|CCL2|COX1|COX2|COX3|CRBN|CXCL1|CYTB|DNM1L|EIF2A|ERAP1|FKBP14|GSTA4|GSTT1|HIF1A|HMGB1|HMOX1|HSPA9|HSPD1|JAK2|KLF13|KRAS|MAOA|MAPRE1|MFF|NCL|ND1|ND5|ND6|NEDD4|NR3C1|NR4A1|PDIA3|PPP2CA|PPP3R1|PROS1|PSMA6|RASA1|STK39|TAP1|TFPI|TFRC|TNFAIP6|UGCG|WDR12|WNK4917/43293 genes: 2.12%

CardiomegalyCardiovascular disease
|Pathology (anatomical condition)
3.31E-060.0044417CASQ2|des|FKTN|GAA|GATAD1|GLRX3|HIF1A|HMOX1|NEXN|PPP3R1|PSEN2|RENBP|ROCK2|SGCD|SIRT4|TRIM63|WDR12168/43293 genes: 0.39%

CardiomyopathiesCardiovascular disease5.17E-060.0069522CASP12|CASQ2|CCL2|COX1|des|FKTN|GAA|GATAD1|HIF1A|HMGB1|HSPD1|NDUFS1|NEXN|PSEN2|RENBP|SGCA|SGCD|SIRT4|TBCA|TFRC|TRIM63|WDR12271/43293 genes: 0.63%

Cerebral small vessel diseasesCardiovascular disease
|Nervous system disease
5.56E-060.007477COX1|COX2|COX3|CYTB|ND1|ND5|ND627/43293 genes: 0.06%