82 phenotypes from 5 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cenpjtm1.1Tkt/Cenpjtm1.1Tkt Not Specified	embryonic lethality between somite formation and embryo turning, complete penetrance	J:184889
Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi B6Brd;B6N-Tyrc-Brd Cenpjtm1a(EUCOMM)Wtsi/Wtsi	abnormal caudal vertebrae morphology	J:194085
	abnormal cell physiology	J:194085
	abnormal ciliary process morphology	J:194085
	abnormal corneal endothelium morphology	J:194085
	abnormal deltoid tuberosity morphology	J:194085
	abnormal dentate gyrus morphology	J:194085
	abnormal Descemet membrane morphology	J:194085
	abnormal double-strand DNA break repair	J:194085
	abnormal glucose tolerance	J:194085
	abnormal humerus morphology	J:194085
	abnormal intramembranous bone ossification	J:194085
	abnormal iridocorneal angle	J:194085
	abnormal iris morphology	J:194085
	abnormal joint morphology	J:194085
	abnormal mitosis	J:194085
	abnormal mitotic spindle morphology	J:194085
	abnormal myocardial fiber morphology	J:194085
	abnormal occipital bone morphology	J:194085
	abnormal parietal bone morphology	J:194085
	abnormal pelvic girdle bone morphology	J:194085
	abnormal retina photoreceptor layer morphology	J:194085
	abnormal social investigation	J:194085
	abnormal sternocostal joint morphology	J:194085
	abnormal thoracic cage morphology	J:194085
	abnormal vertebrae morphology	J:194085
	anophthalmia	J:194085
	normal behavior/neurological phenotype	J:194085
	bowed humerus	J:194085
	caudal vertebral fusion	J:194085
	normal cellular phenotype	J:194085
	chromosomal instability	J:194085
	decreased body length	J:194085
	decreased body size	J:194085
	decreased body weight	J:194085
	decreased brain weight	J:194085
	decreased circulating serum albumin level	J:194085
	decreased cranium length	J:194085
	decreased fetal size	J:194085
	decreased fetal weight	J:194085
	decreased inner canthal distance	J:194085
	decreased neuron number	J:194085
	delayed sexual maturation	J:194085
	eyelids fail to open	J:194085
	increased CD8-positive, alpha-beta T cell number	J:194085
	increased embryonic tissue cell apoptosis	J:194085
	increased T cell number	J:194085
	iris synechia	J:194085
	lethality throughout fetal growth and development, incomplete penetrance	J:194085
	normal nervous system phenotype	J:194085
	polysyndactyly	J:194085
	postnatal growth retardation	J:194085
	prenatal growth retardation	J:194085
	retention of the adrenal gland x-zone	J:194085
	short lumbar vertebrae	J:194085
	sloping forehead	J:194085
	small cranium	J:194085
	small sacral vertebrae	J:194085
	normal taste/olfaction phenotype	J:194085
Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi B6JTyr;B6N-Cenpjtm1a(EUCOMM)Wtsi/Wtsi	abnormal behavior	J:175295
	abnormal cranium morphology	J:175295
	abnormal external male genitalia morphology	J:175295
	abnormal femur morphology	J:175295
	abnormal head morphology	J:175295
	abnormal humerus morphology	J:175295
	abnormal joint morphology	J:175295
	abnormal tail morphology	J:175295
	abnormal tail movements	J:175295
	abnormal tibia morphology	J:175295
	abnormal ulna morphology	J:175295
	abnormal vertebrae morphology	J:175295
	decreased body length	J:175295
	decreased body weight	J:175295
	decreased bone mineral content	J:175295
	decreased circulating calcium level	J:175295
	decreased circulating serum albumin level	J:175295
	decreased circulating total protein level	J:175295
	decreased lean body mass	J:175295
	decreased locomotor activity	J:175295
	decreased total body fat amount	J:175295
	increased sacral vertebrae number	J:175295
	vertebral fusion	J:175295
Cenpjtm1b(EUCOMM)Wtsi/Cenpjtm1b(EUCOMM)Wtsi involves: C57BL/6 * C57BL/6N * FVB/NJ	abnormal embryo development	J:208632
	embryonic growth arrest	J:208632
	embryonic lethality during organogenesis, complete penetrance	J:208632
Cenpjtm1d(EUCOMM)Wtsi/Cenpjtm1c(EUCOMM)Wtsi Tg(Zp3-cre)93Knw/0 involves: C57BL/6J * C57BL/6N * FVB/NJ	abnormal embryo development	J:208632
	embryonic growth arrest	J:208632
	embryonic lethality during organogenesis, complete penetrance	J:208632
Cenpjtm1d(EUCOMM)Wtsi/Cenpjtm1d(EUCOMM)Wtsi involves: C57BL/6 * C57BL/6N * FVB/NJ	abnormal centrosome morphology	J:208632
	abnormal embryo turning	J:208632
	abnormal mitosis	J:208632
	absent embryonic cilia	J:208632
	embryonic growth arrest	J:208632
	embryonic lethality during organogenesis, complete penetrance	J:208632
	increased embryonic tissue cell apoptosis	J:208632