70 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Spred1em1(IMPC)Ccpcz/Spred1em1(IMPC)Ccpcz C57BL/6N-Spred1em1(IMPC)Ccpcz/Ccpcz	abnormal auditory brainstem response	J:211773
	abnormal bone structure	J:211773
	abnormal brain morphology	J:211773
	abnormal cranium morphology	J:211773
	abnormal eye morphology	J:211773
	abnormal head morphology	J:211773
	abnormal head size	J:211773
	abnormal heart morphology	J:211773
	abnormal lymph node morphology	J:211773
	abnormal mandible morphology	J:211773
	abnormal maxilla morphology	J:211773
	abnormal ovary morphology	J:211773
	abnormal retina morphology	J:211773
	abnormal seminal vesicle morphology	J:211773
	abnormal skin coloration	J:211773
	abnormal skin morphology	J:211773
	abnormal snout morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal startle reflex	J:211773
	abnormal thymus morphology	J:211773
	abnormal tooth morphology	J:211773
	abnormal vertebrae morphology	J:211773
	abnormal vertebral arch morphology	J:211773
	abnormal zygomatic bone morphology	J:211773
	anophthalmia	J:211773
	decreased body weight	J:211773
	decreased circulating alkaline phosphatase level	J:211773
	decreased grip strength	J:211773
	decreased locomotor activity	J:211773
	decreased lymphocyte cell number	J:211773
	enlarged heart	J:211773
	enlarged lymph nodes	J:211773
	enlarged spleen	J:211773
	enlarged thymus	J:211773
	fusion of vertebral arches	J:211773
	hydrocephaly	J:211773
	increased CD4-positive NK T cell number	J:211773
	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	J:211773
	increased circulating alanine transaminase level	J:211773
	increased circulating aspartate transaminase level	J:211773
	increased circulating potassium level	J:211773
	increased effector memory CD8-positive, alpha-beta T cell number	J:211773
	increased effector memory T-helper cell number	J:211773
	increased freezing behavior	J:211773
	increased memory-marker CD4-positive NK T cell number	J:211773
	increased neutrophil cell number	J:211773
	increased NK T cell number	J:211773
	increased spleen weight	J:211773
	increased thigmotaxis	J:211773
	small seminal vesicle	J:211773
	tremors	J:211773
	vertebral fusion	J:211773
Spred1tm1.1Ayos/Spred1tm1.1Ayos involves: 129 * C57BL/6 * SJL	normal craniofacial phenotype	J:186742
	increased mast cell degranulation	J:186742
	increased mast cell number	J:186742
Spred1tm1Hiin/Spred1tm1Hiin B6.Cg-Spred1tm1Hiin	abnormal discrimination learning	J:144031
	abnormal excitatory postsynaptic potential	J:144031
	abnormal spatial learning	J:144031
	abnormal spatial working memory	J:144031
	absent long-term depression	J:144031
	enhanced paired-pulse facilitation	J:144031
	impaired swimming	J:144031
	increased thigmotaxis	J:144031
	normal nervous system phenotype	J:144031
	reduced long-term potentiation	J:144031
Spred1tm1Hiin/Spred1tm1Hiin involves: C57BL/6	abnormal cytokine secretion	J:95263
	abnormal eosinophil physiology	J:95263
	decreased body weight	J:95263
	increased airway responsiveness	J:95263
	increased eosinophil cell number	J:95263
	kinked tail	J:95263
	short face	J:95263