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Symbol
Name
ID
Slc5a7
solute carrier family 5 (choline transporter), member 7
MGI:1927126
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Poor suck
Vocal cord paralysis
Vocal cord paresis
Dysphonia
Disease(s) Associated with SLC5A7
congenital myasthenic syndrome 20
distal hereditary motor neuronopathy type 7A

Mouse Phenotypes
increased anxiety-related response
hyporesponsive to tactile stimuli
increased grip strength
hyperactivity
Availability Mouse Genotype
Slc5a7tm1Rbl/Slc5a7tm1Rbl
Slc5a7tm1a(KOMP)Wtsi/Slc5a7+
Tg(Slc5a7)1Rbl/?

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
10/01/2019
MGI 6.14
The Jackson Laboratory