60 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hsd17b4em1(IMPC)Tcp/Hsd17b4+ C57BL/6NCrl-Hsd17b4em1(IMPC)Tcp/Tcp	abnormal seminal vesicle morphology	J:211773
	cataract	J:211773
	decreased circulating aspartate transaminase level	J:211773
	enlarged heart	J:211773
	enlarged urinary bladder	J:211773
	increased grip strength	J:211773
	small uterus	J:211773
Hsd17b4em1(IMPC)Tcp/Hsd17b4em1(IMPC)Tcp C57BL/6NCrl-Hsd17b4em1(IMPC)Tcp/Tcp	abnormal auditory brainstem response	J:211773
	abnormal embryo size	J:211773
	abnormal eye morphology	J:211773
	abnormal gait	J:211773
	abnormal iris morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal sternum morphology	J:211773
	abnormal tooth morphology	J:211773
	enlarged adrenal glands	J:211773
	irregularly shaped pupil	J:211773
	limb grasping	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	small uterus	J:211773
Hsd17b4tm1Baes/Hsd17b4tm1Baes involves: 129S1/Sv * 129X1/SvJ	abnormal bile salt level	J:99925
	abnormal epididymis morphology	J:108368
	abnormal gait	J:201698
	abnormal gametogenesis	J:108368
	abnormal intestinal absorption	J:62314
	abnormal lipid homeostasis	J:104835
	abnormal lipid level	J:62314
	abnormal male germ cell morphology	J:108368
	abnormal male reproductive system morphology	J:108368
	abnormal seminiferous tubule morphology	J:108368
	abnormal spermatid morphology	J:108368
	abnormal spermatogenesis	J:108368
	abnormal testis morphology	J:108368
	astrocytosis	J:201698
	ataxia	J:62314, J:201698
	axon degeneration	J:201698
	cataract	J:62314
	decreased body weight	J:62314
	impaired coordination	J:201698
	increased anxiety-related response	J:201698
	increased fatty acids level	J:201698
	lethargy	J:201698
	male infertility	J:108368
	microgliosis	J:201698
	normal nervous system phenotype	J:104835
	postnatal growth retardation	J:62314
	postnatal lethality, incomplete penetrance	J:62314
	premature death	J:201698
	Purkinje cell degeneration	J:201698
	reduced male fertility	J:62314
	seminiferous tubule degeneration	J:108368
	small testis	J:108368
	tremors	J:201698
Hsd17b4tm2Baes/Hsd17b4tm2Baes involves: 129 * C57BL/6	no abnormal phenotype detected	J:201698
Hsd17b4tm2Baes/Hsd17b4tm2Baes Cnptm1(cre)Kan/Cnp+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	normal behavior/neurological phenotype	J:201698
	normal growth/size/body region phenotype	J:201698
	increased fatty acids level	J:201698
	normal nervous system phenotype	J:201698
	normal reproductive system phenotype	J:201698
Hsd17b4tm2Baes/Hsd17b4tm2Baes Tg(Nes-cre)1Kln/0 involves: 129 * C57BL/6 * SJL	abnormal gait	J:201698
	ataxia	J:201698
	axon degeneration	J:201698
	cerebellum atrophy	J:201698
	decreased body weight	J:201698
	decreased litter size	J:201698
	demyelination	J:201698
	impaired coordination	J:201698
	increased anxiety-related response	J:201698
	increased fatty acids level	J:201698
	male infertility	J:201698
	microgliosis	J:201698
	neuron degeneration	J:201698
	postnatal growth retardation	J:201698
	premature death	J:201698
	Purkinje cell degeneration	J:201698
	reduced female fertility	J:201698
	short stride length	J:201698
	tremors	J:201698