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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Spag17
sperm associated antigen 17
MGI:1921612
43 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Spag17tm1b(KOMP)Wtsi/Spag17tm1b(KOMP)Wtsi
B6N(Cg)-Spag17tm1b(KOMP)Wtsi/J
abnormal cauda epididymis morphology J:264221
abnormal intramanchette transport J:264221
abnormal manchette assembly J:264221
abnormal outer dense fiber morphology J:264221
abnormal sperm axoneme morphology J:264221
abnormal sperm head morphology J:264221
abnormal sperm nucleus morphology J:264221
abnormal spermiogenesis J:264221
absent sperm fibrous sheath J:264221
absent sperm head J:264221
arrest of spermatogenesis J:264221
detached acrosome J:264221
elongated manchette J:264221
immotile sperm J:264221
male infertility J:264221
oligozoospermia J:264221
pregnancy-related premature death J:264221
normal reproductive system phenotype J:264221
short sperm flagellum J:264221
thin sperm flagellum J:264221
Spag17tm1b(KOMP)Wtsi/Spag17tm1b(KOMP)Wtsi
C57BL/6N-Spag17tm1b(KOMP)Wtsi/J
decreased body length J:211773
limb grasping J:211773
male infertility J:211773
Spag17tm1c(KOMP)Wtsi/Spag17+
involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
no abnormal phenotype detected J:211752
Spag17tm1c(KOMP)Wtsi/Spag17tm1c(KOMP)Wtsi
involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
prenatal lethality, complete penetrance J:211752
Spag17tm1d(KOMP)Wtsi/Spag17+
involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
no abnormal phenotype detected J:211752
Spag17tm1d(KOMP)Wtsi/Spag17tm1d(KOMP)Wtsi
involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
abnormal pulmonary alveolus epithelium morphology J:211752
abnormal respiratory motile cilium morphology J:211752
abnormal respiratory motile cilium physiology J:211752
abnormal suckling behavior J:211752
absent gastric milk in neonates J:211752
atelectasis J:211752
cyanosis J:211752
decreased heart rate J:211752
decreased locomotor activity J:211752
enlarged brain ventricles J:211752
enlarged lateral ventricles J:211752
normal growth/size/body region phenotype J:211752
hydrocephaly J:211752
immotile respiratory cilia J:211752
impaired mucociliary clearance J:211752
neonatal lethality, complete penetrance J:211752
pulmonary edema J:211752
respiratory distress J:211752
respiratory failure J:211752

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory