57 phenotypes from 7 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hip1em1(IMPC)Hmgu/Hip1em1(IMPC)Hmgu C57BL/6N-Hip1em1(IMPC)Hmgu/Ieg	abnormal cornea morphology	J:211773
	abnormal gait	J:211773
	abnormal vertebrae morphology	J:211773
	corneal opacity	J:211773
	decreased body length	J:211773
	decreased circulating creatinine level	J:211773
	decreased locomotor activity	J:211773
	decreased vertical activity	J:211773
	hyperactivity	J:211773
	increased bone mineral content	J:211773
Hip1tm1Hay/Hip1tm1Hay involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal gait	J:84278
	abnormal motor capabilities/coordination/movement	J:84278
	abnormal muscle morphology	J:84278
	decreased body weight	J:84278
	decreased locomotor activity	J:84278
	kyphosis	J:84278
	postnatal growth retardation	J:84278
	premature death	J:84278
	short stride length	J:84278
	tremors	J:84278
Hip1tm1Tsr/Hip1+ involves: 129X1/SvJ * C57BL/6	seminiferous tubule degeneration	J:72637
Hip1tm1Tsr/Hip1tm1Tsr involves: 129X1/SvJ * C57BL/6	abnormal seminiferous tubule morphology	J:90400
	abnormal spermatogenesis	J:72637
	absent common myeloid progenitor cells	J:90400
	normal behavior/neurological phenotype	J:72637
	decreased male germ cell number	J:72637
	decreased testis weight	J:72637
	normal hematopoietic system phenotype	J:90400
	normal homeostasis/metabolism phenotype	J:72637
	increased male germ cell apoptosis	J:72637
	multinucleated giant male germ cells	J:90400
	oligozoospermia	J:72637
	postnatal lethality, incomplete penetrance	J:72637
	seminiferous tubule degeneration	J:72637
	testicular atrophy	J:72637
	normal vision/eye phenotype	J:90400
Hip1tm2.1Tsr/Hip1tm2.1Tsr involves: 129X1/SvJ	normal hematopoietic system phenotype	J:90400
	kyphosis	J:90400
	male infertility	J:90400
	normal skeleton phenotype	J:90400
	normal vision/eye phenotype	J:90400
Hip1tm2Tsr/Hip1tm2Tsr involves: 129X1/SvJ * C57BL/6	no abnormal phenotype detected	J:90400
Hip1tm3Tsr/Hip1tm3Tsr involves: 129X1/SvJ * C57BL/6	abnormal spermatid morphology	J:90400
	absent common myeloid progenitor cells	J:90400
	normal hematopoietic system phenotype	J:90400
	lordokyphosis	J:90400
	microphthalmia	J:90400
	normal nervous system phenotype	J:90400
	nuclear cataract	J:90400
	perinatal lethality, incomplete penetrance	J:90400
	reduced male fertility	J:90400
	normal skeleton phenotype	J:90400
	small lens	J:90400
	testis degeneration	J:90400
	weight loss	J:90400
Hip1tm4Tsr/Hip1+ involves: 129X1/SvJ * C57BL/6	cataract	J:151974
	microphthalmia	J:151974
Hip1tm4Tsr/Hip1+ Tg(Mx1-cre)1Cgn/0 involves: 129X1/SvJ * C57BL/6 * CBA	abnormal myelopoiesis	J:151974
	abnormal spleen morphology	J:151974
	abnormal tumor incidence	J:151974
	decreased hematopoietic stem cell number	J:151974
	enlarged spleen	J:151974
	normal hematopoietic system phenotype	J:151974
	increased hepatocellular carcinoma incidence	J:151974
	increased liver tumor incidence	J:151974
	increased spleen red pulp amount	J:151974
	increased susceptibility to xenobiotic induced morbidity/mortality	J:151974
	increased T cell derived lymphoma incidence	J:151974