Symbol Name ID |
Slc5a7
solute carrier family 5 (choline transporter), member 7 MGI:1927126 |
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/? |
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, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/07/2024 MGI 6.23 |
|
|