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Phenotypes Associated with This Genotype
Genotype
MGI:4818488
Allelic
Composition		 Slc6a9tm1Veul/Slc6a9tm1Veul
Tg(Syn1-cre)671Jxm/?
Genetic
Background		 involves: 129P2/OlaHsd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc6a9tm1Veul mutation (0 available); any Slc6a9 mutation (24 available)
Tg(Syn1-cre)671Jxm mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
muscle
muscle phenotype ( J:161993 )
N
• no hypotonia

behavior/neurological
behavior/neurological phenotype ( J:161993 )
N
• no motor defects seen in open field or rotarod tests

nervous system
abnormal neuron physiology ( J:161993 )
• GlyT1 specific uptake of glycine by hippocampal membranes is reduced 50%

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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Send questions and comments to User Support. 		last database update
05/21/2024
MGI 6.23 		The Jackson Laboratory