About   Help   FAQ
Symbol
Name
ID
Slc5a7
solute carrier family 5 (choline transporter), member 7
MGI:1927126
Phenotype annotations related to respiratory system
Darker colors indicate more annotations
Human Phenotypes
Stridor
Apnea
Hypoventilation
Disease(s) Associated with SLC5A7
congenital myasthenic syndrome 20

Mouse Phenotypes
respiratory failure
Availability Mouse Genotype
Slc5a7tm1Rbl/Slc5a7tm1Rbl

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 & Copyright Notice
Send questions and comments to User Support.
last database update
08/13/2019
MGI 6.14
The Jackson Laboratory