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

Mouse Phenotypes
abnormal eye morphology
retrolental blood
Availability Mouse Genotype
Slc5a7tm1a(KOMP)Wtsi/Slc5a7tm1a(KOMP)Wtsi

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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last database update
02/05/2019
MGI 6.13
The Jackson Laboratory