41 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rnd3Gt(IST12405G10)Tigm/Rnd3Gt(IST12405G10)Tigm involves: C57BL/6N	abnormal brain ependyma morphology	J:197325
	abnormal brain ventricular system morphology	J:197325
	abnormal cerebral aqueduct morphology	J:197325
	cerebral aqueductal stenosis	J:197325
	dilated third ventricle	J:197325
	domed cranium	J:197325
	enlarged lateral ventricles	J:197325
	hydrocephaly	J:197325
Rnd3Gt(OST364657)Lex/Rnd3Gt(OST364657)Lex involves: 129S5/SvEvBrd * C57BL/6J	abnormal ear development	J:172361
	abnormal gait	J:172361
	abnormal hypaxial muscle morphology	J:172361
	abnormal limb posture	J:172361
	abnormal locomotor behavior	J:172361
	abnormal motor capabilities/coordination/movement	J:172361
	abnormal neuromuscular synapse morphology	J:172361
	abnormal pinna reflex	J:172361
	abnormal placing response	J:172361
	abnormal sciatic nerve morphology	J:172361
	abnormal spinal nerve morphology	J:172361
	abnormal tibialis anterior morphology	J:172361
	ataxia	J:172361
	behavioral developmental delay	J:172361
	convulsive seizures	J:172361
	decreased birth body size	J:172361
	decreased grip strength	J:172361
	decreased locomotor activity	J:172361
	decreased motor neuron number	J:172361
	delayed eyelid opening	J:172361
	delayed suckling reflex loss	J:172361
	impaired righting response	J:172361
	limb grasping	J:172361
	positive geotaxis	J:172361
	postnatal growth retardation	J:172361
	postnatal lethality, incomplete penetrance	J:172361
	premature death	J:172361
	short stride length	J:172361
	slow postnatal weight gain	J:172361
	weight loss	J:172361
Rnd3tm1b(EUCOMM)Hmgu/Rnd3+ C57BL/6N-Rnd3tm1b(EUCOMM)Hmgu/H	decreased grip strength	J:211773
	enlarged heart	J:211773
	increased large unstained cell number	J:211773
	polycystic kidney	J:211773