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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
T(16;17)43H
reciprocal translocation, Chr 16 and 17, Harwell 43
MGI:3574967
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ot1
T(16;17)43H/0 involves: 101 * C3H * PWD/Ph MGI:3575502


Genotype
MGI:3575502
ot1
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
• 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





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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
12/10/2024
MGI 6.24
The Jackson Laboratory