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Symbol
Name
ID

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

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Delayed skeletal maturation	Pathologic fracture	Recurrent fractures	Osteopenia	Osteoporosis
Disease(s) Associated with SLC7A7
lysinuric protein intolerance

Mouse Phenotypes		abnormal skeleton development	decreased bone mineralization
Availability	Mouse Genotype	abnormal skeleton development	decreased bone mineralization
	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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