54 phenotypes from 5 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gt(ROSA)26Sortm5(CAG-Sun1/sfGFP)Nat/Gt(ROSA)26Sortm5(CAG-Sun1/sfGFP)Nat involves: 129 * C57BL/6	no abnormal phenotype detected	J:101977
Sun1em1Leim/Sun1em1Leim C57BL/6-Sun1em1Leim	abnormal meiotic attachment of telomere to nuclear envelope	J:270644
Sun1tm1.1Ktj/Sun1tm1.1Ktj involves: 129/Sv * C57BL/6 * C57BL/6N	abnormal cerebellar foliation	J:224769
	abnormal cerebellum development	J:224769
	abnormal cerebellum external granule cell layer morphology	J:224769
	abnormal Purkinje cell migration	J:224769
	abnormal Purkinje cell morphology	J:224769
	absent cerebellum fissure	J:224769
	ataxia	J:224769
	decreased brain weight	J:224769
	ectopic Purkinje cell	J:224769
	impaired coordination	J:224769
	small cerebellum	J:224769
Sun1tm1.1Ktj/Sun1tm1.1Ktj involves: C57BL/6J * FVB/N	abnormal male meiosis	J:146636
	absent oocytes	J:146636
	absent ovarian follicles	J:146636
	arrest of male meiosis	J:146636
	azoospermia	J:146636
	decreased testis weight	J:146636
	female infertility	J:146636
	male infertility	J:146636
	small testis	J:146636
Sun1tm1.1Ktj/Sun1tm1.1Ktj Not Specified	abnormal male meiosis	J:194067
	ataxia	J:224769
Sun1tm1b(EUCOMM)Wtsi/Sun1tm1b(EUCOMM)Wtsi C57BL/6N-Sun1tm1b(EUCOMM)Wtsi/Orl	abnormal auditory brainstem response	J:211773
	abnormal retina morphology	J:211773
	abnormal retina outer nuclear layer morphology	J:211773
	abnormal startle reflex	J:211773
	decreased circulating serum albumin level	J:211773
	decreased circulating total protein level	J:211773
	decreased lean body mass	J:211773
	decreased locomotor activity	J:211773
	decreased lymphocyte cell number	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	decreased total retina thickness	J:211773
	female infertility	J:211773
	increased circulating phosphate level	J:211773
	increased heart rate	J:211773
	increased leukocyte cell number	J:211773
	increased lymphocyte cell number	J:211773
	increased monocyte cell number	J:211773
	increased neutrophil cell number	J:211773
	increased total body fat amount	J:211773
	male infertility	J:211773
	small superior vagus ganglion	J:211773
	small testis	J:211773
Sun1tm1Mhan/Sun1tm1Mhan B6.129S6-Sun1tm1Mhan	abnormal male meiosis	J:205574
	abnormal meiotic attachment of telomere to nuclear envelope	J:205574
Sun1tm1Mhan/Sun1tm1Mhan involves: 129S6/SvEvTac	abnormal chromosomal synapsis	J:122602
	abnormal cochlear outer hair cell morphology	J:194486
	abnormal female meiosis	J:122602
	abnormal muscle morphology	J:150047
	abnormal spermatocyte morphology	J:122602
	absent oocytes	J:122602
	absent ovarian follicles	J:122602
	absent pinna reflex	J:194486
	arrest of male meiosis	J:122602
	cochlear outer hair cell degeneration	J:194486
	decreased male germ cell number	J:122602
	female infertility	J:122602
	increased or absent threshold for auditory brainstem response	J:194486
	increased ovary apoptosis	J:122602
	increased testis apoptosis	J:122602
	male infertility	J:122602
	small ovary	J:122602
	small testis	J:122602
Sun1tm1Mhan/Sun1tm1Mhan involves: 129S6/SvEvTac * C57BL/6J	abnormal chromosomal synapsis	J:209347
	abnormal male meiosis	J:209347