abnormal synaptic dopamine release Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant secretion across synapses of the catecholamine neurotransmitter and neurohormone, derived from tyrosine and the precursor to norepinephrine and epinephrine; functions as a neurotransmitter in the brain and as a hormone to inhibit the release of prolactin from the anterior lobe of the pituitary (Mammalian Phenotype Ontology, MP_0010149)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010149
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Genes

3 gene mutations causing the abnormal synaptic dopamine release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3D1 adaptor-related protein complex 3, delta 1 subunit
CHRM5 cholinergic receptor, muscarinic 5
CHRNA4 cholinergic receptor, nicotinic, alpha 4 (neuronal)