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Symbol
Name
ID
Slc18a1
solute carrier family 18 (vesicular monoamine), member 1
MGI:106684
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Negativism
Disease(s) Associated with SLC18A1
schizophrenia

Mouse Phenotypes
behavior/neurological phenotype
abnormal object recognition memory
Availability Mouse Genotype
Slc18a1tm1Dgen/Slc18a1tm1Dgen *

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory