| 377 |
abnormal |
regulation of gene expression
(GO:0010468)
|
|
1214: Altered gene expression specific to CAR activation, Hepatocytes
|
| 427 |
abnormal |
signaling
(GO:0023052)
|
hypoxia-inducible factor 1-alpha
(PR:000008555)
|
801: modulation, Unknown
|
| 490 |
abnormal |
vasodilation
(GO:0042311)
|
blood vessel
(UBERON:0001981)
|
937: KE7 : Impaired, Vasodilation
|
| 491 |
abnormal |
antioxidant activity
(GO:0016209)
|
glutathione
(CHEBI:16856)
|
926: Oxidation, Glutathione (To be considered with MIE)
|
| 495 |
abnormal |
cardiovascular system development
(GO:0072358)
|
cardiovascular system
(UBERON:0004535)
|
317: Altered, Cardiovascular development/function
|
| 511 |
abnormal |
ovulation cycle
(GO:0042698)
|
|
971: Ovulation of oocytes Reduced, Delayed, or Blocked, Decrease or delay in LH surge required for ovulation
|
| 550 |
abnormal |
lipid metabolic process
(GO:0006629)
|
|
1060: Alteration, lipid metabolism
|
| 578 |
abnormal |
role
(MESH:D012380)
|
|
1108: Abnormal, Role change within caste
|
| 580 |
abnormal |
hemostasis
(GO:0007599)
|
|
1122: Under carboxylated clotting factors will not assemble on cell surfaces to form clot, Failure of secondary hemostasis
|
| 581 |
abnormal |
wound healing
(GO:0042060)
|
|
1130: Failure in vascular repair mechanisms, Unresolved blood loss (hemorrhage)
|
| 587 |
abnormal |
cellular detoxification
(GO:1990748)
|
|
1132: Blood loss and development of anemia, Impaired oxygen delivery and nutrient delivery to tissue, impaired carbon dioxide and waste product removal
|
| 591 |
abnormal |
vitamin K metabolic process
(GO:0042373)
|
vitamin K
(CHEBI:28384)
|
1134: Irreversible inhibition of hepatic VKOR by binding of AR at tyrosine 139, Failure to cycle vitamin K epoxide to vitamin K to form vitamin K hydroquinone
|
| 601 |
abnormal |
post-translational protein modification
(GO:0043687)
|
osteocalcin
(PR:000030444)
|
1169: Anticoagulant rodenticide interferes with carboxylation of Gla proteins in bone, Impairment of post-translational modification (carboxylation) of osteocalcin
|
| 651 |
abnormal |
gene expression
(GO:0010467)
|
|
1239: Altered, Gene Expression
|
| 652 |
abnormal |
translation
(GO:0006412)
|
protein
(PR:000000001)
|
1240: Altered, Protein Production
|
| 660 |
abnormal |
|
Food Chain
(MESH:D020387)
|
1210: Alteration, Food-web structures
|
| 661 |
abnormal |
DNA topoisomerase II activity
(GO:0061505)
|
|
1252: Binding to (interferes with) topoisomerase II enzyme
|
| 663 |
abnormal |
cellular component organization
(GO:0016043)
|
|
1258: Decompartmentalization
|
| 665 |
abnormal |
plasma membrane organization
(GO:0007009)
|
|
1259: narcosis
|
| 679 |
abnormal |
|
cholesterol
(CHEBI:16113)
|
1289: Perturbation of cholesterol
|
| 680 |
abnormal |
|
glutathione
(CHEBI:16856)
|
1290: Glutathione homeostasis
|
| 683 |
abnormal |
signaling
(GO:0023052)
|
Wnt signalosome
(GO:1990909)
|
1294: Inhibition, Wnt pathway
|
| 684 |
abnormal |
embryo development
(GO:0009790)
|
|
1295: Defect of Embryogenesis
|
| 708 |
abnormal |
chemical synaptic transmission
(GO:0007268)
|
synapse
(GO:0045202)
|
758: Hippocampal Physiology, Altered
|
| 733 |
abnormal |
Abnormal spermatogenesis
(HP:0008669)
|
Mature sperm cell
(FMA:67338)
|
1758: Impaired, Spermatogenesis
|