54 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Trip13em1(IMPC)J/Trip13em1(IMPC)J C57BL/6NJ-Trip13em1(IMPC)J/J	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	female infertility	J:211773
	male infertility	J:211773
Trip13Gt(CH0621)Wtsi/Trip13Gt(CH0621)Wtsi involves: 129P2/OlaHsd * C57BL/6	abnormal chiasmata formation	J:163309
	abnormal chromosomal synapsis	J:163309
	abnormal female meiosis	J:163309
	abnormal seminiferous tubule morphology	J:163309
	abnormal synaptonemal complex	J:163309
	arrest of male meiosis	J:163309
	impaired ovarian folliculogenesis	J:163309
	infertility	J:163309
	small testis	J:163309
Trip13Gt(RRB047)Byg/Trip13Gt(RRB047)Byg involves: 129P2/OlaHsd * C57BL/6	abnormal chiasmata formation	J:163309
	abnormal chromosomal synapsis	J:163309
	abnormal DNA repair	J:123677
	abnormal double-strand DNA break repair	J:123677, J:163309
	abnormal female meiosis	J:123677, J:163309
	abnormal ovary morphology	J:123677
	abnormal seminiferous tubule morphology	J:163309
	abnormal synaptonemal complex	J:163309
	absent ovarian follicles	J:123677
	arrest of male meiosis	J:123677, J:163309
	decreased body size	J:123677
	decreased oocyte number	J:123677
	immotile sperm	J:123677
	impaired ovarian folliculogenesis	J:163309
	infertility	J:123677, J:163309
	kinked tail	J:123677
	postnatal lethality, incomplete penetrance	J:123677
	short tail	J:123677
	small gonad	J:123677
	small ovary	J:123677
	small testis	J:123677, J:163309
Trip13tm1.1(KOMP)Vlcg/Trip13+ C57BL/6N-Trip13tm1.1(KOMP)Vlcg/Ucd	abnormal retina morphology	J:211773
	increased anxiety-related response	J:211773
	increased circulating alkaline phosphatase level	J:211773
Trip13tm1.1(KOMP)Vlcg/Trip13tm1.1(KOMP)Vlcg C57BL/6N-Trip13tm1.1(KOMP)Vlcg/Ucd	abnormal bone structure	J:211773
	abnormal coat/hair pigmentation	J:211773
	abnormal digit morphology	J:211773
	abnormal iris pigmentation	J:211773
	abnormal lens morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal tail morphology	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased erythrocyte cell number	J:211773
	decreased grip strength	J:211773
	decreased hematocrit	J:211773
	decreased hemoglobin content	J:211773
	decreased lean body mass	J:211773
	decreased locomotor activity	J:211773
	female infertility	J:211773
	hyperactivity	J:211773
	increased blood urea nitrogen level	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating HDL cholesterol level	J:211773
	increased circulating serum albumin level	J:211773
	increased fasting circulating glucose level	J:211773
	increased leukocyte cell number	J:211773
	increased mean corpuscular hemoglobin	J:211773
	increased thigmotaxis	J:211773
	increased total body fat amount	J:211773
	increased vertical activity	J:211773
	male infertility	J:211773
	persistence of hyaloid vascular system	J:211773
	prolonged RR interval	J:211773