32 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Plcb4tm1b(EUCOMM)Wtsi/Plcb4tm1b(EUCOMM)Wtsi C57BL/6N-Plcb4tm1b(EUCOMM)Wtsi/Tcp	abnormal auditory brainstem response	J:211773
	abnormal gait	J:211773
	abnormal gallbladder morphology	J:211773
	abnormal locomotor behavior	J:211773
	abnormal uterus morphology	J:211773
	decreased exploration in new environment	J:211773
	decreased locomotor activity	J:211773
	decreased total body fat amount	J:211773
	enlarged gallbladder	J:211773
	hydrometra	J:211773
	increased bone mineral content	J:211773
	increased grip strength	J:211773
	increased lean body mass	J:211773
	increased vertical activity	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Plcb4tm1Dwu/Plcb4tm1Dwu involves: 129S1/Sv	abnormal locomotor coordination	J:51664
	abnormal Purkinje cell innervation	J:51664
	abnormal rod electrophysiology	J:77638
	abnormal vision	J:77638
	ataxia	J:51664
	impaired coordination	J:51664
	short stride length	J:51664
Plcb4tm1Hssh/Plcb4tm1Hssh Not Specified	abnormal cerebellar foliation	J:43077
	abnormal cerebellum external granule cell layer morphology	J:43077
	abnormal gait	J:43077
	abnormal synaptic transmission	J:43077
	ataxia	J:43077
	decreased body size	J:43077
	decreased locomotor activity	J:43077
	normal muscle phenotype	J:43077
	postnatal lethality, incomplete penetrance	J:43077
	normal skeleton phenotype	J:43077
	small cerebellum	J:43077
Plcb4tm1Tyo/Plcb4tm1Tyo involves: C57BL/6J	abnormal nervous system physiology	J:72939
	reduced long-term depression	J:72939