78 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kcnj10tm1b(KOMP)Wtsi/Kcnj10+ C57BL/6N-Kcnj10tm1b(KOMP)Wtsi/H	decreased basophil cell number	J:211773
	decreased exploration in new environment	J:211773
	decreased mean platelet volume	J:211773
	increased startle reflex	J:211773
	tremors	J:211773
Kcnj10tm1b(KOMP)Wtsi/Kcnj10tm1b(KOMP)Wtsi C57BL/6N-Kcnj10tm1b(KOMP)Wtsi/H	preweaning lethality, complete penetrance	J:211773
Kcnj10tm1Kdmc/Kcnj10tm1Kdmc Tg(GFAP-cre)1Kdmc/? involves: 129S6/SvEvTac * C3H * C57BL/6 * C57BL/6J * SJL	abnormal astrocyte morphology	J:126082
	abnormal astrocyte physiology	J:126082
	abnormal CNS glial cell morphology	J:126082
	abnormal CNS synaptic transmission	J:126082
	abnormal excitatory postsynaptic currents	J:126082
	abnormal eye physiology	J:126082
	abnormal motor capabilities/coordination/movement	J:126082
	abnormal nervous system morphology	J:126082
	abnormal nervous system physiology	J:126082
	abnormal oligodendrocyte morphology	J:126082
	abnormal spinal cord white matter morphology	J:126082
	ataxia	J:126082
	brain vacuoles	J:126082
	decreased body size	J:126082
	decreased brain size	J:126082
	delayed eyelid opening	J:126082
	dilated lateral ventricle	J:126082
	enhanced long-term potentiation	J:126082
	eyelids fail to open	J:126082
	gliosis	J:126082
	hindlimb paralysis	J:126082
	impaired righting response	J:126082
	increased post-tetanic potentiation	J:126082
	lethargy	J:126082
	premature death	J:126082
	slow postnatal weight gain	J:126082
	thin cerebral cortex	J:126082
	tonic-clonic seizures	J:126082
	tremors	J:126082
Kcnj10tm1Lst/Kcnj10+ involves: 129S1/Sv * C57BL/6J	abnormal eye physiology	J:63635
Kcnj10tm1Lst/Kcnj10tm1Lst involves: 129S1/Sv	abnormal renal tubule morphology	J:226598
	decreased urine calcium level	J:226598
	decreased urine creatinine level	J:226598
	increased urine sodium level	J:226598
	polyuria	J:226598
	postnatal growth retardation	J:226598
	postnatal lethality, complete penetrance	J:226598
Kcnj10tm1Lst/Kcnj10tm1Lst involves: 129S1/Sv * C57BL/6J	abnormal cochlea morphology	J:108878
	abnormal cochlear endolymph ionic homeostasis	J:75599
	abnormal cochlear nerve morphology	J:108878
	abnormal crista ampullaris neuroepithelium morphology	J:108878
	abnormal eye electrophysiology	J:63635
	abnormal motor capabilities/coordination/movement	J:77663
	abnormal motor coordination/balance	J:63635, J:77663
	abnormal myelination	J:77663
	abnormal nervous system electrophysiology	J:77663
	abnormal oligodendrocyte morphology	J:77663
	abnormal posture	J:77663
	abnormal Reissner membrane morphology	J:75599, J:108878
	abnormal scala media morphology	J:108878
	abnormal spinal cord morphology	J:77663
	abnormal spinal cord white matter morphology	J:77663
	abnormal stria vascularis morphology	J:108878
	abnormal tectorial membrane morphology	J:108878
	absent endocochlear potential	J:75599
	absent pinna reflex	J:75599
	absent startle reflex	J:108878
	axon degeneration	J:77663
	cochlear ganglion degeneration	J:108878
	cochlear inner hair cell degeneration	J:108878
	cochlear outer hair cell degeneration	J:108878
	collapsed Reissner membrane	J:108878
	decreased body size	J:63635, J:77663
	decreased body weight	J:77663
	dehydration	J:77663
	distended Reissner membrane	J:108878
	normal hearing/vestibular/ear phenotype	J:75599
	hindlimb paralysis	J:77663
	impaired balance	J:63635
	impaired hearing	J:75599
	impaired righting response	J:108878
	increased or absent threshold for auditory brainstem response	J:75599
	jerky movement	J:63635
	organ of Corti degeneration	J:108878
	postnatal growth retardation	J:63635, J:77663, J:108878
	postnatal lethality, complete penetrance	J:63635, J:77663, J:108878
	tremors	J:77663
	utricular macular degeneration	J:108878
	vestibular ganglion degeneration	J:108878
	vestibular hair cell degeneration	J:108878
	vestibular saccular macula degeneration	J:108878
	normal vision/eye phenotype	J:63635
	weakness	J:77663