About   Help   FAQ
Symbol
Name
ID
Slc7a7
solute carrier family 7 (cationic amino acid transporter, y+ system), member 7
MGI:1337120
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Abnormal heart morphology
Hepatosplenomegaly
Disease(s) Associated with SLC7A7
lysinuric protein intolerance

Mouse Phenotypes
ventricular septal defect
cardiac hypertrophy
Availability Mouse Genotype
Slc7a7em1(IMPC)Bay/Slc7a7em1(IMPC)Bay

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
07/02/2024
MGI 6.13
The Jackson Laboratory