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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Synj2
synaptojanin 2
MGI:1201671
13 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Synj2mozart/Synj2mozart
C57BL/6-Synj2mozart
normal behavior/neurological phenotype J:171701
cochlear ganglion degeneration J:171701
cochlear hair cell degeneration J:171701
cochlear inner hair cell degeneration J:171701
cochlear outer hair cell degeneration J:171701
fused inner hair cell stereocilia J:171701
fused outer hair cell stereocilia J:171701
impaired hearing J:171701
increased or absent threshold for auditory brainstem response J:171701
normal nervous system phenotype J:171701
organ of Corti degeneration J:171701
sensorineural hearing loss J:171701
Synj2mozart/Synj2mozart
involves: BALB/c * C57BL/6
impaired hearing J:171701
Synj2mozart/Synj2mozart
involves: C57BL/6 * CBA/H
impaired hearing J:171701
increased or absent threshold for auditory brainstem response J:171701
Synj2tm1a(EUCOMM)Wtsi/Synj2tm1a(EUCOMM)Wtsi
C57BL/6N-Synj2tm1a(EUCOMM)Wtsi/Wtsi
increased body weight J:165965

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
09/10/2019
MGI 6.14
The Jackson Laboratory