increased serotonin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the amount of biochemical messenger and regulator, found in the CNS, gastrointestinal tract, and produced by platelets that mediates neurotransmission, gastrointestinal motility, hemostasis, and cardiovascular integrity (Mammalian Phenotype Ontology, MP_0010069)
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9 gene mutations causing the increased serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRL3 adhesion G protein-coupled receptor L3
GSTM5 glutathione S-transferase mu 5
MAGED1 melanoma antigen family D1
MPST mercaptopyruvate sulfurtransferase
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8
STX1A syntaxin 1A (brain)
TAAR1 trace amine associated receptor 1
TDO2 tryptophan 2,3-dioxygenase
UBE3A ubiquitin protein ligase E3A