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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
autosomal dominant distal hereditary motor neuronopathy 7
congenital myasthenic syndrome 20

Mouse Phenotypes
increased anxiety-related response
hyporesponsive to tactile stimuli
increased grip strength
increased locomotor activity
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
05/07/2024
MGI 6.23
The Jackson Laboratory