Symbol
Name
ID

Slc18a2
solute carrier family 18 (vesicular monoamine), member 2
MGI:106677

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Temperature instability	Elevated urinary homovanillic acid
Disease(s) Associated with SLC18A2	Temperature instability	Elevated urinary homovanillic acid
infantile parkinsonism-dystonia 2

Mouse Phenotypes

increased susceptibility to dopaminergic neuron neurotoxicity

decreased body temperature

abnormal catecholamine level

abnormal dopamine level

decreased dopamine level

abnormal noradrenaline level

abnormal corticosterone level

abnormal serotonin level

decreased serotonin level

abnormal enzyme/coenzyme activity

decreased physiological sensitivity to xenobiotic

Availability

Mouse Genotype

Slc18a2^tm1Edw/Slc18a2^tm1Edw

Slc18a2^tm1Mca/Slc18a2^tm1Mca

Slc18a2^tm2Kmo/Slc18a2^tm2Kmo

Slc18a2^tm1Edw/Slc18a2⁺

Slc18a2^tm1Mca/Slc18a2⁺

Slc18a2^tm1Uhl/Slc18a2⁺

Slc18a2^tm1.1Bgir/Slc18a2^tm1.1Bgir
Slc6a4^tm1(cre)Xz/Slc6a4⁺ (conditional)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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