Synj2 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Synj2^mozart/Synj2^mozart C57BL/6-Synj2^mozart	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
Synj2^mozart/Synj2^mozart involves: BALB/c * C57BL/6	impaired hearing	J:171701
Synj2^mozart/Synj2^mozart involves: C57BL/6 * CBA/H	impaired hearing	J:171701
Synj2^mozart/Synj2^mozart involves: C57BL/6 * CBA/H	increased or absent threshold for auditory brainstem response	J:171701
Synj2^{tm1a(EUCOMM)Wtsi}/Synj2^{tm1a(EUCOMM)Wtsi} C57BL/6N-Synj2^{tm1a(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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