Phenotypes for T(16;17)43H MGI:3575502 MGI Mouse

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Phenotypes Associated with This Genotype

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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