45 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Katnb1taily/Katnb1taily involves: C57BL/6 * CBA	abnormal male meiosis	J:185194
	abnormal manchette disassembly	J:185194
	abnormal manchette morphology	J:185194
	abnormal manchette perinuclear ring morphology	J:185194
	abnormal meiotic spindle morphology	J:185194
	abnormal outer dense fiber morphology	J:185194
	abnormal sperm axoneme morphology	J:185194
	abnormal sperm flagellum morphology	J:185194
	abnormal spermatid morphology	J:185194
	absent sperm axonemal central pair	J:185194
	asthenozoospermia	J:185194
	decreased sperm progressive motility	J:185194
	elongated manchette	J:185194
	globozoospermia	J:185194
	increased Sertoli cell phagocytosis	J:185194
	male infertility	J:185194
	oligozoospermia	J:185194
	normal reproductive system phenotype	J:185194
	small testis	J:185194
Katnb1tm1a(EUCOMM)Hmgu/Katnb1tm1a(EUCOMM)Hmgu C57BL/6-Katnb1tm1a(EUCOMM)Hmgu	abnormal cell cytoskeleton morphology	J:220901
	abnormal cell morphology	J:220901
	abnormal cortical ventricular zone morphology	J:220901
	abnormal embryo morphology	J:220901
	abnormal erythropoiesis	J:220901
	abnormal forebrain morphology	J:220901
	abnormal mitosis	J:220901
	abnormal mitotic spindle morphology	J:220901
	abnormal neuronal precursor proliferation	J:220901
	abnormal primary cilium morphology	J:220901
	aneuploidy	J:220901
	anophthalmia	J:220901
	binucleate	J:220901
	decreased brain size	J:220901
	decreased embryo size	J:220901
	decreased fibroblast proliferation	J:220901
	decreased neuronal precursor cell number	J:220901
	holoprosencephaly	J:220901
	increased brain apoptosis	J:220901
	lethality throughout fetal growth and development, complete penetrance	J:220901
	loss of cortex neurons	J:220901
	microphthalmia	J:220901
	pale liver	J:220901
	small limb buds	J:220901
	thin cerebral cortex	J:220901
Katnb1tm1b(EUCOMM)Hmgu/Katnb1tm1b(EUCOMM)Hmgu C57BL/6N-Katnb1tm1b(EUCOMM)Hmgu/H	preweaning lethality, complete penetrance	J:211773