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Symbol
Name
ID
Slc5a7
solute carrier family 5 (choline transporter), member 7
MGI:1927126
Phenotype annotations related to digestive/alimentary system
Darker colors indicate more annotations
Human Phenotypes
Dysphagia
Disease(s) Associated with SLC5A7
congenital myasthenic syndrome 20

Mouse Phenotypes
dilated pancreatic duct
abnormal small intestine morphology
Availability Mouse Genotype
Slc5a7tm1a(KOMP)Wtsi/Slc5a7tm1a(KOMP)Wtsi

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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last database update
08/13/2019
MGI 6.14
The Jackson Laboratory