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Mammalian Phenotype Ontology Annotations
Query Results - Summary
SH3 and multiple ankyrin repeat domains 1
22 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
abnormal gait J:211773
cataract J:211773
decreased eosinophil cell number J:211773
decreased exploration in new environment J:211773
decreased freezing behavior J:211773
decreased startle reflex J:211773
increased lymphocyte cell number J:211773
increased mean corpuscular hemoglobin concentration J:211773
tremors J:211773
involves: 129S4/SvJae * C57BL/6
abnormal CNS synapse formation J:132277
abnormal CNS synaptic transmission J:132277
abnormal hippocampus pyramidal cell morphology J:132277
abnormal long term spatial reference memory J:132277
abnormal maternal nurturing J:132277
abnormal spatial learning J:132277
abnormal spatial reference memory J:132277
abnormal spatial working memory J:132277
hypoactivity J:132277
impaired coordination J:132277
increased anxiety-related response J:132277
normal nervous system phenotype J:132277
reduced fertility J:132277

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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last database update
MGI 6.16
The Jackson Laboratory