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Phenotypes Associated with This Genotype
Genotype
MGI:3575502
Allelic
Composition		 T(16;17)43H/0
Genetic
Background		 involves: 101 * C3H * PWD/Ph
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
T(16;17)43H mutation (1 available); any T(16;17)43H mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
behavior/neurological
abnormal spatial learning ( J:97039 )
• 12 month old mutant mice show significant deficit of spatial learning in the Morris water maze test

Mouse Models of Human Disease
 DO ID OMIM ID(s) Ref(s)
chromosomal disease DOID:0080014 J:97039
Down syndrome DOID:14250 OMIM:190685
 J:208905

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
11/05/2024
MGI 6.24 		The Jackson Laboratory