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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Sun1
Sad1 and UNC84 domain containing 1
MGI:1924303
53 phenotypes from 5 alleles in 9 genetic backgrounds
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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 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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory