44 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Srrm4bv/Srrm4bv involves: 129	abnormal cochlear inner hair cell morphology	J:31165
	cochlear inner hair cell degeneration	J:31165
Srrm4bv/Srrm4bv Not Specified	abnormal cochlear hair cell development	J:39922
	abnormal cochlear inner hair cell morphology	J:6106, J:13866
	abnormal crista ampullaris morphology	J:13866
	abnormal distortion product otoacoustic emission	J:117755
	abnormal hearing electrophysiology	J:32693
	abnormal inner ear morphology	J:13866, J:28889
	abnormal otoacoustic response	J:32693
	abnormal pillar cell morphology	J:6106
	abnormal pinna reflex	J:6106
	abnormal utricular macula morphology	J:28889
	abnormal vestibular hair cell morphology	J:28889
	absent cochlear inner hair cells	J:6106
	absent pillar cells	J:6106
	absent vestibular hair cell stereocilia	J:193641
	circling	J:39922
	cochlear ganglion degeneration	J:6106
	cochlear inner hair cell degeneration	J:39922
	deafness	J:6106, J:13866, J:193641
	decreased cochlear inner hair cell number	J:193641
	decreased vestibular hair cell number	J:193641
	head tossing	J:39922
	impaired balance	J:193641
	increased or absent threshold for auditory brainstem response	J:117755
	utricular macular degeneration	J:28889
Srrm4bv/Srrm4bv Tg(Myo7a-Srrm4)#Bban/0 Not Specified	normal behavior/neurological phenotype	J:193641
	normal hearing/vestibular/ear phenotype	J:193641
Srrm4tm1b(EUCOMM)Wtsi/Srrm4+ involves: C57BL/6J * C57BL/6N	abnormal axon guidance	J:221584
	abnormal stratification in cerebral cortex	J:221584
Srrm4tm1b(EUCOMM)Wtsi/Srrm4tm1b(EUCOMM)Wtsi involves: C57BL/6J * C57BL/6N	abnormal axon extension	J:221584
	abnormal axon guidance	J:221584
	abnormal corpus callosum morphology	J:221584
	abnormal embryonic/fetal subventricular zone morphology	J:221584
	abnormal innervation	J:221584
	abnormal neurite morphology	J:221584
	abnormal phrenic nerve innervation pattern to diaphragm	J:221584
	abnormal stratification in cerebral cortex	J:221584
	circling	J:221584
	cyanosis	J:221584
	decreased neuron number	J:221584
	decreased neuronal precursor cell number	J:221584
	decreased survivor rate	J:221584
	head tilt	J:221584
	neonatal lethality, incomplete penetrance	J:221584
	premature neuronal precursor differentiation	J:221584
	respiratory distress	J:221584
	tremors	J:221584
Srrm4tm1e(EUCOMM)Wtsi/Srrm4tm1e(EUCOMM)Wtsi C57BL/6N-Srrm4tm1e(EUCOMM)Wtsi/Wtsi	preweaning lethality, incomplete penetrance	J:211773
	tremors	J:211773