Symbol
Name
ID

Slc7a7
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
MGI:1337120

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes

Decreased circulating antibody level

Increased circulating antibody level

Increased serum zinc

Elevated plasma citrulline

Hypolysinemia

Hyperglutaminemia

Hyperprolinemia

Hyperglycinemia

Abnormal circulating serine concentration

Hyperalaninemia

Decreased HDL cholesterol concentration

Increased LDL cholesterol concentration

Hypercholesterolemia

Hypertriglyceridemia

Hyperammonemia

Increased circulating ferritin concentration

Elevated circulating hepatic transaminase concentration

Increased circulating lactate dehydrogenase concentration

Increased circulating lactate concentration

Oroticaciduria

Proteinuria

Aminoaciduria

Hyperlysinuria

Argininuria

Ornithinuria

Hepatic amyloidosis

Renal amyloidosis

Disease(s) Associated with SLC7A7

lysinuric protein intolerance

Mouse Phenotypes		argininuria	lysinuria	aminoaciduria	increased circulating ammonia level
Availability	Mouse Genotype	argininuria	lysinuria	aminoaciduria	increased circulating ammonia level
	Slc7a7^em1Lbu/Slc7a7^em1Lbu
	Slc7a7^{Gt(OST41878)Lex}/Slc7a7^{Gt(OST41878)Lex}

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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