42 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Wdr62em1(IMPC)Tcp/Wdr62em1(IMPC)Tcp C57BL/6NCrl-Wdr62em1(IMPC)Tcp/Tcp	decreased prepulse inhibition	J:211773
	enlarged lymph nodes	J:211773
	increased circulating sodium level	J:211773
	male infertility	J:211773
	microphthalmia	J:211773
	small kidney	J:211773
	small seminal vesicle	J:211773
	small testis	J:211773
Wdr62Gt(AF0003)Wtsi/Wdr62Gt(AF0003)Wtsi involves: 129P2/OlaHsd * 129S1/SvImJ	abnormal mitosis	J:224504
	abnormal mitotic spindle assembly checkpoint	J:224504
	abnormal mitotic spindle morphology	J:224504
	abnormal nervous system physiology	J:224504
	decreased neuronal precursor cell number	J:224504
	fetal growth retardation	J:224504
	increased cell death	J:224504
	loss of cortex neurons	J:224504
	microcephaly	J:224504
	proportional dwarf	J:224504
	reduced fertility	J:224504
	thin cerebral cortex	J:224504
Wdr62tm1.1Jfch/Wdr62tm1.1Jfch involves: 129S1/SvImJ * C57BL/6N	abnormal cell cycle	J:282438
	abnormal neocortex size	J:282438
	abnormal primary cilium morphology	J:282438
	decreased brain size	J:282438
	decreased brain weight	J:282438
	decreased cell proliferation	J:282438
	decreased neuronal precursor cell number	J:282438
	increased forebrain apoptosis	J:282438
	premature neuronal precursor differentiation	J:282438
Wdr62tm3a(EUCOMM)Hmgu/Wdr62tm3a(EUCOMM)Hmgu C57BL/6-Wdr62tm3a(EUCOMM)Hmgu	abnormal cortical ventricular zone morphology	J:306320
	abnormal male meiosis	J:306320
	abnormal manchette disassembly	J:306320
	abnormal neocortex morphology	J:306320
	abnormal seminiferous tubule morphology	J:306320
	abnormal sperm head morphology	J:306320
	absent oocytes	J:306320
	asthenozoospermia	J:306320
	decreased sperm progressive motility	J:306320
	decreased testis weight	J:306320
	female infertility	J:306320
	normal growth/size/body region phenotype	J:306320
	male infertility	J:306320
	oligozoospermia	J:306320
	small testis	J:306320
	teratozoospermia	J:306320
	thin cerebral cortex	J:306320