31 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Pou4f2tm3Whk/Pou4f2tm3Whk Pou4f3tm1Whk/Pou4f3tm1Whk Not Specified	abnormal retina ganglion cell morphology	J:73779
	abnormal retina morphology	J:73779
	abnormal retina nerve fiber layer morphology	J:73779
	abnormal sensory neuron innervation pattern	J:73779
	abnormal vestibular system physiology	J:73779
	deafness	J:73779
	decreased retina ganglion cell number	J:73779
	increased amacrine cell number	J:73779
	thin retina ganglion layer	J:73779
Pou4f3em1(cre/ERT2)Yss/Pou4f3+ Tmem63bem2Yss/Tmem63bem2Yss involves: C57BL/6N	abnormal distortion product otoacoustic emission	J:303483
	cochlear outer hair cell degeneration	J:303483
	impaired hearing	J:303483
	increased or absent threshold for auditory brainstem response	J:303483
Pou4f3tm1.1(HBEGF)Jsto/Pou4f3+ either: (involves: 129S4/SvJaeSor * C57BL/6) or (involves: 129S4/SvJaeSor * CBA/J)	abnormal gait	J:191218
	abnormal motor capabilities/coordination/movement	J:191218
	abnormal utricle morphology	J:191218
	abnormal vestibular hair cell morphology	J:191218
	abnormal vestibular hair cell stereociliary bundle morphology	J:191218
	abnormal vestibular system physiology	J:191218
	circling	J:191218
	decreased vestibular hair cell number	J:191218
	head bobbing	J:191218
	premature death	J:191218
	weight loss	J:191218
Pou4f3tm1.1(HBEGF)Rubel/Pou4f3+ involves: 129S4/SvJaeSor * C57BL/6J * CBA/J	abnormal cochlear ganglion morphology	J:240454
	absent cochlear inner hair cells	J:240454
	absent cochlear outer hair cells	J:240454
	cochlear ganglion degeneration	J:240454
	conductive hearing loss	J:240454
	deafness	J:240454
	mixed hearing loss	J:240454
	sensorineural hearing loss	J:240454
	small cochlear ganglion	J:240454