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Symbol
Name
ID

Slc52a3
solute carrier protein family 52, member 3
MGI:1916948

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Vocal cord paralysis	Weak voice
Disease(s) Associated with SLC52A3	Vocal cord paralysis	Weak voice
Brown-Vialetto-Van Laere syndrome 1

Mouse Phenotypes		lethargy	decreased food intake	hunched posture
Availability	Mouse Genotype	lethargy	decreased food intake	hunched posture
	Slc52a3^{tm2a(KOMP)Wtsi}/Slc52a3^{tm2a(KOMP)Wtsi}
	Slc52a3^tm1.1Said/Slc52a3^tm1.1Said Tg(Vil1-cre)997Gum/0 (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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